Allele Registry

Canonical Allele Identifier: PA2828916002

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056771

RCV001316353

ClinVar Variation:

16832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369639.1:p.Asn343del	CA217012 NM_001382710.1:c.1028_1030del