Canonical Allele Identifier: PA2828916473
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 16832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Asn359del
CA217012
NM_001382711.1:c.1076_1078del