21645-7

LOINC 2.82

CACNA1S gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

CACNA1S gene Mut Tested Bld/T

Component

  • CACNA1S gene mutations tested for

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; CACH1; CACN1; CACNL1A3; calcium channel, voltage-dependent, L type, alpha 1S subunit; Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit; Cav1.1; CCHL1A3; DHP receptor; Gene mut tested; Genetics; Heredity; Heritable; HOKPP; HOKPP1; Hypokalemic periodic paralysis; HypoPP; Identity or presence; Inherited; Malignant hyperthermia susceptibility 5; MHS5; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Tested; Mutation; Muts; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; TTPP1; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • CACH1
  • CACN1
  • CACNL1A3
  • calcium channel, voltage-dependent, L type, alpha 1S subunit
  • Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
  • Cav1.1
  • CCHL1A3
  • DHP receptor
  • Gene mut tested
  • Genetics
  • Heredity
  • Heritable
  • HOKPP
  • HOKPP1
  • Hypokalemic periodic paralysis
  • HypoPP
  • Identity or presence
  • Inherited
  • Malignant hyperthermia susceptibility 5
  • MHS5
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Tested
  • Mutation
  • Muts
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • TTPP1
  • WB
  • Whole blood
  • Whole blood or Tissue