Allele Registry

Canonical Allele Identifier: PA331209

Gene: MSH2 HGNC NCBI

MaveDb:

Score 2.5125481427

ClinVar RCV:

RCV000076002

RCV001213427

ClinVar Variation:

90507

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu341Pro	CA016875 NM_000251.3:c.1022T>C