Canonical Allele Identifier: PA2828914963
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1305123
ClinVar RCV Id: RCV001773833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Ile123Asn
CA350685594
NM_001382708.1:c.368T>A