Canonical Allele Identifier: PA2828917335
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 16832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Asn276del
CA217012
NM_001382713.1:c.827_829del