43747-5

LOINC 2.82

OCA2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

OCA2 gene Mut Anl Bld/T

Component

  • OCA2 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • BEY; BEY1; BEY2; Blood; BOCA; D15S12; EYCL; EYCL2; EYCL3; Genetics; HCL3; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; Oculocutaneous albinism II; P; P protein gene; PCR; PED; Point in time; Random; SHEP1; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • BEY
  • BEY1
  • BEY2
  • Blood
  • BOCA
  • D15S12
  • EYCL
  • EYCL2
  • EYCL3
  • Genetics
  • HCL3
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • OCA2 gene targeted mutation analysis
  • Oculocutaneous albinism II
  • P
  • P protein gene
  • PCR
  • PED
  • Point in time
  • Random
  • SHEP1
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue