| Approved symbol | RAI1 |
|---|---|
| Approved name | retinoic acid induced 1 |
| HGCN ID | HGNC:9834 |
| Previous symbols | SMCR |
| Inheritance | |
| OMIM | 607642 |
| Chromosome | 17p11.2 |
| Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Mendelioom |
| Approved symbol | RAI1 |
|---|---|
| Approved name | retinoic acid induced 1 |
| HGCN ID | HGNC:9834 |
| Previous symbols | SMCR |
| Inheritance | |
| OMIM | 607642 |
| Chromosome | 17p11.2 |
| Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Mendelioom |