Allele Registry

Canonical Allele Identifier: PA2829599033

Gene: HADH HGNC NCBI

ClinVar RCV:

RCV000153344

RCV001513868

ClinVar Variation:

167162

HGVS (amino-acid)	Matching Registered Transcripts
NP_005318.6:p.Leu86Pro	CA180095 NM_005327.7:c.257T>C