Allele Registry

Canonical Allele Identifier: PA2828917158

Gene: DES HGNC NCBI

ClinVar RCV:

RCV003797372

ClinVar Variation:

2940014

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369642.1:p.Glu100Gly	CA350685021 NM_001382713.1:c.299A>G