Canonical Allele Identifier: PA2828915452
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1002861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Ala135Gly
CA350685921
NM_001382709.1:c.404C>G