| Approved symbol | PRF1 |
|---|---|
| Approved name | perforin 1 |
| HGCN ID | HGNC:9360 |
| Previous symbols | |
| Inheritance | |
| OMIM | 170280 |
| Chromosome | 10q22.1 |
| Panel(s) |
NGS Epilepsy NGS Hemophagocytic syndrome (HLH) NGS Hereditary cancer panel 2 NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID |
