Allele Registry

Canonical Allele Identifier: PA915954396

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000807667

ClinVar Variation:

652165

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg711Gly	CA346729287 NM_000251.3:c.2131C>G