Allele Registry

Canonical Allele Identifier: PA645474248

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000216853

RCV001072003

RCV001800565

ClinVar Variation:

232572

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val417Gly	CA10577969 NM_000251.3:c.1250T>G