Canonical Allele Identifier: PA916070965
Gene: DHDDS HGNC NCBI

Linked Data

ClinVar Variation Id: 451635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995583.1:p.Arg37His
CA339138678
NM_205861.3:c.110G>A