Canonical Allele Identifier: PA2828915807
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1718790
ClinVar RCV Id: RCV002301696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Ala134Glu
CA350685894
NM_001382710.1:c.401C>A