| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | CPT2-related disorder +14 more | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyltransferase II deficiency +10 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene