Allele Registry

Canonical Allele Identifier: PA2826464095

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000507809

RCV000541857

RCV000572189

RCV000986669

RCV004003546

ClinVar Variation:

439186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg378His	CA346724650 NM_001258281.1:c.1133G>A