Allele Registry

Canonical Allele Identifier: PA133852

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000037241

RCV000528546

RCV000618538

RCV000726980

RCV000735343

RCV001798112

RCV002504889

ClinVar Variation:

44261

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Leu136His	CA133850 NM_001927.4:c.407T>A