Allele Registry

Canonical Allele Identifier: PA299429

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160665

RCV000206352

RCV000565934

RCV000656894

RCV000662428

RCV000708864

RCV001030492

RCV002484997

ClinVar Variation:

182620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Tyr397Cys	CA008291 NM_000179.3:c.1190A>G