Allele Registry

Canonical Allele Identifier: PA2826464286

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160587

RCV000573867

RCV000821313

RCV003998471

ClinVar Variation:

182560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr429Ala	CA018401 NM_001258281.1:c.1285A>G