Allele Registry

Canonical Allele Identifier: PA299309

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160583

RCV000198641

RCV000492025

RCV000662679

RCV002265636

RCV003998470

ClinVar Variation:

182558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp461Ala	CA018117 NM_000251.3:c.1382A>C