| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CACNA1A, LOC126862865 (T1331I +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA1A, LOC126862865 (F1327fs +2 more) | Indel (frameshift variant) | Inborn genetic diseases | |
Click to view in NCBI Gene