Allele Registry

Canonical Allele Identifier: PA2826463844

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000569958

RCV000985791

RCV001858301

RCV003459358

ClinVar Variation:

483715

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp320Gly	CA346733699 NM_001258281.1:c.959A>G