Allele Registry

Canonical Allele Identifier: PA658672227

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000569958

RCV000985791

RCV001858301

RCV003459358

ClinVar Variation:

483715

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp386Gly	CA346733699 NM_000251.3:c.1157A>G