Allele Registry

Canonical Allele Identifier: PA2499230024

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001295164

ClinVar Variation:

999199

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln395Glu	CA346733845 NM_000251.3:c.1183C>G