Allele Registry

Canonical Allele Identifier: PA2826626292

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001982099

RCV003289257

ClinVar Variation:

1432785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe443Leu	CA346748631 NM_001281492.2:c.1327T>C CA346748664 NM_001281492.2:c.1329T>A CA346748667 NM_001281492.2:c.1329T>G