Allele Registry

Canonical Allele Identifier: PA645474983

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000226382

RCV001013729

RCV003998759

ClinVar Variation:

237379

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile651Val	CA10582019 NM_000251.3:c.1951A>G