| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861868, ATP11A (A1021T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATP11A, LOC126861868 (H1025Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene