| Approved symbol | SMARCE1 |
|---|---|
| Approved name | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 |
| HGCN ID | HGNC:11109 |
| Previous symbols | |
| Inheritance | |
| OMIM | 603111 |
| Chromosome | 17q21.2 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Hereditary cancer panel 2 NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |
