| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130008908, PRKAB1 (D39E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130008908, PRKAB1 (L46F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene