Canonical Allele Identifier: PA100550
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 66404
ClinVar RCV Id: RCV000056792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ser460Ile
CA217051
NM_001927.4:c.1379G>T