Allele Registry

Canonical Allele Identifier: PA2825091853

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001971716

RCV002458921

ClinVar Variation:

1477689

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1193Ala	CA346760508 NM_000179.3:c.3578A>C