| Approved symbol | ASXL3 |
|---|---|
| Approved name | ASXL transcriptional regulator 3 |
| HGCN ID | HGNC:29357 |
| Previous symbols | KIAA1713 |
| Inheritance | |
| OMIM | 615115 |
| Chromosome | 18q12.1 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly |
