Allele Registry

Canonical Allele Identifier: PA2826465197

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000629899

RCV002420671

RCV004002780

ClinVar Variation:

525696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala644Gly	CA034290 NM_001258281.1:c.1931C>G