Canonical Allele Identifier: PA2828915792
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2450698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Ala120Gly
CA350685502
NM_001382710.1:c.359C>G