Canonical Allele Identifier: PA2499259739
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1002861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ala135Gly
CA350685921
NM_001927.4:c.404C>G