Allele Registry

Canonical Allele Identifier: PA2826632818

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

138594

ClinVar RCV:

RCV000121586

RCV000200854

RCV000214188

RCV000590417

RCV000663151

RCV003460855

RCV003997353

ClinVar Variation:

134855

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Val776Ala	CA012103 NM_001281493.2:c.2327T>C