Allele Registry

Canonical Allele Identifier: PA160915

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000121586

RCV000200854

RCV000214188

RCV000590417

RCV000663151

RCV003460855

RCV003997353

ClinVar Variation:

134855

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val1078Ala	CA012103 NM_000179.3:c.3233T>C