| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | NALCN-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | NALCN-related disorder +1 more | GPathogenic/Likely pathogenic |
| | LOC126861831, NALCN (Y386* +1 more) | Single nucleotide variant (nonsense) | NALCN-related disorder | |
Click to view in NCBI Gene