Allele Registry

Canonical Allele Identifier: PA2826466014

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 584611

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Phe856Leu	CA346732054 NM_001258281.1:c.2566T>C CA346732064 NM_001258281.1:c.2568T>A CA346732071 NM_001258281.1:c.2568T>G