| Approved symbol | STX1B |
|---|---|
| Approved name | syntaxin 1B |
| HGCN ID | HGNC:18539 |
| Previous symbols | STX1B1, STX1B2 |
| Inheritance | |
| OMIM | 601485 |
| Chromosome | 16p11.2 |
| Panel(s) |
NGS Epilepsy NGS Fetal akinesia deformation sequence FADS NGS Intellectual disability NGS Mendeliome |
