| Approved symbol | ARID1B |
|---|---|
| Approved name | AT-rich interaction domain 1B |
| HGCN ID | HGNC:18040 |
| Previous symbols | |
| Inheritance | |
| OMIM | 614556 |
| Chromosome | 6q25.3 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |
