Allele Registry

Canonical Allele Identifier: PA2826632855

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000222192

RCV000536806

RCV000562792

RCV001174616

RCV003998628

ClinVar Variation:

234562

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro784Leu	CA10577285 NM_001281493.2:c.2351C>T