Canonical Allele Identifier: PA2828916951
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1212419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Ile367Val
CA2125240
NM_001382712.1:c.1099A>G