| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862611, TLK2 (N171T +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862611, TLK2 (I336L +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene