Canonical Allele Identifier: PA916070990
Gene: DHDDS HGNC NCBI

Linked Data

ClinVar Variation Id: 488193
ClinVar RCV Id: RCV000578123 RCV001853833 RCV001172209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995583.1:p.Arg211Gln
CA339144815
NM_205861.3:c.632G>A