| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936895, PRKCD (Q127R +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129936895, PRKCD (M116I +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene