Allele Registry

Canonical Allele Identifier: PA2573165082

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 1400256

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Phe608Leu	CA346728356 NM_000251.3:c.1822T>C CA346728361 NM_000251.3:c.1824T>G CA346728362 NM_000251.3:c.1824T>A