Allele Registry

Canonical Allele Identifier: PA645381065

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000215890

RCV000225881

RCV000569553

RCV000662360

RCV003998620

RCV004541361

ClinVar Variation:

234483

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly620Ser	CA10577265 NM_000179.3:c.1858G>A