38921-3LOINC 2.82
MSH6 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
MSH6 gene Mut Anl Bld/T
Component
- MSH6 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; G/T mismatch-binding protein gene; Genetics; GTBP; GTMBP; Heredity; Heritable; HNPCC; HNPCC5; HSAP; Identity or presence; Inherited; Lynch syndrome; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; mutS homolog 6; Nominal; p160; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- G/T mismatch-binding protein gene
- Genetics
- GTBP
- GTMBP
- Heredity
- Heritable
- HNPCC
- HNPCC5
- HSAP
- Identity or presence
- Inherited
- Lynch syndrome
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MSH6 gene targeted mutation analysis
- Mut
- Mut Anl
- Mutations
- mutS homolog 6
- Nominal
- p160
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue