Allele Registry

Canonical Allele Identifier: PA110901

Gene: DHDDS HGNC NCBI

ClinVar RCV:

RCV000023687

RCV000762902

RCV000778978

RCV001354833

ClinVar Variation:

30709

HGVS (amino-acid)	Matching Registered Transcripts
NP_995583.1:p.Lys42Glu	CA259894 NM_205861.3:c.124A>G