Allele Registry

Canonical Allele Identifier: PA645470881

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.7793915078

ClinVar RCV:

RCV000219790

RCV000235807

RCV000473744

RCV000663256

ClinVar Variation:

232346

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln4Leu	CA027207 NM_000251.3:c.11A>T