Canonical Allele Identifier: PA2828916269
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1051933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Leu136Val
CA350685931
NM_001382711.1:c.406C>G