| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | NPM2, LOC124153117 (S133I +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC124153117, NPM2 (A149T +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene