Allele Registry

Canonical Allele Identifier: PA2826142453

Gene: HADH HGNC NCBI

ClinVar RCV:

RCV000153344

RCV001513868

ClinVar Variation:

167162

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171634.3:p.Leu86Pro	CA180095 NM_001184705.4:c.257T>C