Canonical Allele Identifier: PA100340
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 66390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ala357Pro
CA217007
NM_001927.4:c.1069G>C