Allele Registry

Canonical Allele Identifier: PA2579919425

Gene: MSH2 HGNC NCBI

MaveDb:

Score -6.2453384272

ClinVar RCV:

RCV003165204

ClinVar Variation:

2447350

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala636Thr	CA346728614 NM_000251.3:c.1906G>A