Allele Registry

Canonical Allele Identifier: PA645475575

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.6258006425

ClinVar RCV:

RCV000477479

RCV002446812

ClinVar Variation:

408498

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp758Asn	CA16611050 NM_000251.3:c.2272G>A