Canonical Allele Identifier: PA2499259738
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1055317
ClinVar RCV Id: RCV001363964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg127Gly
CA350685715
NM_001927.4:c.379C>G