Allele Registry

Canonical Allele Identifier: PA217014

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056771

RCV001316353

ClinVar Variation:

16832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Asn366del	CA217012 NM_001927.4:c.1097_1099del