Allele Registry

Canonical Allele Identifier: PA645474977

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000222363

RCV000523371

RCV000629936

RCV001355204

RCV003469093

RCV003998593

ClinVar Variation:

234021

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile648Asn	CA032124 NM_000251.3:c.1943T>A