Allele Registry

Canonical Allele Identifier: PA658673173

Gene: MSH2 HGNC NCBI

MaveDb:

Score -1.4088397284

ClinVar RCV:

RCV000566548

ClinVar Variation:

480959

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu881Lys	CA346731335 NM_000251.3:c.2641G>A