| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936565, NKTR
+1 more (Y439C +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129936565, NKTR
+1 more (S555Y +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129936565, NKTR
+1 more (N588S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129936565, NKTR
+1 more (R483G +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene