Allele Registry

Canonical Allele Identifier: PA658674261

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000546121

ClinVar Variation:

474285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Pro419Thr	CA350696531 NM_001927.4:c.1255C>A