| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | ATP1A3-associated neurological disorder +4 more | |
| | | Single nucleotide variant (missense variant) | ATP1A3-associated neurological disorder +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | ATP1A3-associated neurological disorder | |
Click to view in NCBI Gene