Allele Registry

Canonical Allele Identifier: PA100442

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056780

RCV001064294

ClinVar Variation:

66397

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Glu401Lys	CA284671 NM_001927.4:c.1201G>A