Allele Registry

Canonical Allele Identifier: PA645497879

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000491641

RCV001701986

ClinVar Variation:

265811

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Leu136Pro	CA350685955 NM_001927.4:c.407T>C