Allele Registry

Canonical Allele Identifier: PA2826463464

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131729

RCV000487151

RCV001182806

RCV001202065

ClinVar Variation:

142539

922624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met234Ile	CA022513 NM_001258281.1:c.702G>A CA346732941 NM_001258281.1:c.702G>C CA346732942 NM_001258281.1:c.702G>T