Allele Registry

Canonical Allele Identifier: PA915964304

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001012805

ClinVar Variation:

819882

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly571Ser	CA346748571 NM_000179.3:c.1711G>A