| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130009747, SUCLA2 (A27V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | LOC130009747, SUCLA2 (T23R) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
Click to view in NCBI Gene