| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129995124, NIPAL4 (P20S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995124, NIPAL4 (P20H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant) | Inborn genetic diseases | |
Click to view in NCBI Gene