Allele Registry

Canonical Allele Identifier: PA658745800

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000583013

RCV002279366

RCV003465313

RCV003758864

ClinVar Variation:

491885

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly620Cys	CA346749808 NM_000179.3:c.1858G>T