Allele Registry

Canonical Allele Identifier: PA2826462825

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 91044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu27Phe	CA020925 NM_001258281.1:c.79C>T