| Approved symbol | SMC1A |
|---|---|
| Approved name | structural maintenance of chromosomes 1A |
| HGCN ID | HGNC:11111 |
| Previous symbols | SMC1L1 |
| Inheritance | |
| OMIM | 300040 |
| Chromosome | Xp11.22 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia SMC1A Analysis |
