| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129930598, USP24 (G75R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129930598, USP24 (P70S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene