Canonical Allele Identifier: PA110901
Gene: DHDDS HGNC NCBI

Linked Data

ClinVar Variation Id: 30709
ClinVar RCV Id: RCV000023687 RCV000762902 RCV000778978 RCV001354833
JSON-LD

Amino-acid Alleles

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