Canonical Allele Identifier: PA2826328561
Gene: DHDDS HGNC NCBI

Linked Data

ClinVar Variation Id: 30709
ClinVar RCV Id: RCV000023687 RCV000762902 RCV000778978 RCV001354833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230494.1:p.Lys42Glu
CA259894
NM_001243565.2:c.124A>G