Allele Registry

Canonical Allele Identifier: PA645472955

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000457800

RCV000575104

RCV000663211

RCV000852299

RCV001584155

ClinVar Variation:

408558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala328Thr	CA16610859 NM_000251.3:c.982G>A