Canonical Allele Identifier: PA915975708
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 636840
ClinVar RCV Id: RCV000788786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Glu111Gly
CA350685299
NM_001927.4:c.332A>G