Allele Registry

Canonical Allele Identifier: PA645475359

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000490880

RCV000659883

RCV000664310

RCV001209603

ClinVar Variation:

428464

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly692Trp	CA346729189 NM_000251.3:c.2074G>T