| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130056046, PAPLN (G82S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130056046, PAPLN (A83S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130056046, PAPLN (R84Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene