Allele Registry

Canonical Allele Identifier: PA2826626498

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000583013

RCV002279366

RCV003465313

RCV003758864

ClinVar Variation:

491885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly490Cys	CA346749808 NM_001281492.2:c.1468G>T