Allele Registry

Canonical Allele Identifier: PA094773

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076384

RCV002228184

RCV002415564

RCV004537293

ClinVar Variation:

90882

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Cys697Arg	CA019984 NM_000251.3:c.2089T>C