| Approved symbol | NOTCH2 |
|---|---|
| Approved name | notch receptor 2 |
| HGCN ID | HGNC:7882 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600275 |
| Chromosome | 1p12 |
| Panel(s) |
NGS Congenitale hartafwijkingen NGS Mendelioom NGS Skeletdysplasie |
| Approved symbol | NOTCH2 |
|---|---|
| Approved name | notch receptor 2 |
| HGCN ID | HGNC:7882 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600275 |
| Chromosome | 1p12 |
| Panel(s) |
NGS Congenitale hartafwijkingen NGS Mendelioom NGS Skeletdysplasie |