Canonical Allele Identifier: PA2828916949
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 16832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Asn366del
CA217012
NM_001382712.1:c.1097_1099del