Allele Registry

Canonical Allele Identifier: PA2828915165

Gene: DES HGNC NCBI

ClinVar RCV:

RCV003802665

ClinVar Variation:

2941643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369637.1:p.Leu337Arg	CA216999 NM_001382708.1:c.1010T>G CA2740096450 NM_001382708.1:c.1010_1011delinsGC