Allele Registry

Canonical Allele Identifier: PA645509846

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.6526948578

ClinVar RCV:

RCV000506535

RCV000630170

RCV001764503

RCV002329207

RCV003470639

ClinVar Variation:

439195

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala15Thr	CA346728542 NM_000251.3:c.43G>A