Allele Registry

Canonical Allele Identifier: PA891844732

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 584611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Phe922Leu	CA346732054 NM_000251.3:c.2764T>C CA346732064 NM_000251.3:c.2766T>A CA346732071 NM_000251.3:c.2766T>G