Canonical Allele Identifier: PA2828917385
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2090670
ClinVar RCV Id: RCV002991421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Glu322Asp
CA350695096
NM_001382713.1:c.966G>C
CA350695098
NM_001382713.1:c.966G>T