| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126805580, PLCH2 (P828L +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PLCH2, LOC126805580 (Q823H +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene