Allele Registry

Canonical Allele Identifier: PA2826464281

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 408482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln427Leu	CA028775 NM_001258281.1:c.1280A>T