Canonical Allele Identifier: PA2828915279
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2922193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Thr462Ile
CA350699035
NM_001382708.1:c.1385C>T