Allele Registry

Canonical Allele Identifier: PA2826628855

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115419

RCV000122966

RCV000212687

RCV000588959

RCV000659895

RCV001005027

RCV001081954

RCV001358662

ClinVar Variation:

127589

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr1113Ser	CA014099 NM_001281492.2:c.3337A>T