Allele Registry

Canonical Allele Identifier: PA916011361

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000464681

RCV000483362

RCV000491614

RCV000662364

RCV001354888

RCV001368829

RCV004001848

ClinVar Variation:

237182

410497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly939Arg	CA070372 NM_001281492.2:c.2815G>C CA10582082 NM_001281492.2:c.2815G>A