Allele Registry

Canonical Allele Identifier: PA658679959

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000575294

RCV000689038

RCV000985851

RCV001292699

ClinVar Variation:

485853

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn21Asp	CA346734569 NM_000179.3:c.61A>G