| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861831, NALCN (E417K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126861831, NALCN (Y377D +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126861831, NALCN (I370M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126861831, NALCN (T395A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene