| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861611, UTP20 (V540I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861611, UTP20 (G554E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene