| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806224, USP34 (P1802Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806224, USP34 (D1784N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806224, USP34 (D1776A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806224, USP34 (L1775F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806224, USP34 (R1770Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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