Allele Registry

Canonical Allele Identifier: PA284675

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056782

RCV000685786

ClinVar Variation:

66398

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Glu413Lys	CA284673 NM_001927.4:c.1237G>A