Allele Registry

Canonical Allele Identifier: PA2826463641

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001995910

RCV002378356

ClinVar Variation:

1482973

1757437

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg274Ser	CA346733161 NM_001258281.1:c.822A>C CA346733163 NM_001258281.1:c.822A>T