Allele Registry

Canonical Allele Identifier: PA645475009

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000217308

RCV001301645

RCV003462530

ClinVar Variation:

233706

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile667Val	CA10577992 NM_000251.3:c.1999A>G