Allele Registry

Canonical Allele Identifier: PA357588

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000663023

RCV001320681

ClinVar Variation:

220628

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly338Ala	CA349698 NM_000251.3:c.1013G>C