Allele Registry

Canonical Allele Identifier: PA163839

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000129124

RCV000210186

RCV000688403

RCV003477537

ClinVar Variation:

140888

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn477His	CA018266 NM_000251.3:c.1429A>C