Canonical Allele Identifier: PA102026
Gene: HADHA HGNC NCBI

Linked Data

ClinVar Variation Id: 100085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000173.2:p.Glu510Gln
CA119870
NM_000182.5:c.1528G>C