Allele Registry

Canonical Allele Identifier: PA2573164958

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001995910

RCV002378356

ClinVar Variation:

1482973

1757437

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg340Ser	CA346733161 NM_000251.3:c.1020A>C CA346733163 NM_000251.3:c.1020A>T