| Approved symbol | TCF4 |
|---|---|
| Approved name | transcription factor 4 |
| HGCN ID | HGNC:11634 |
| Previous symbols | |
| Inheritance | |
| OMIM | 602272 |
| Chromosome | 18q21.2 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly |
| Approved symbol | TCF4 |
|---|---|
| Approved name | transcription factor 4 |
| HGCN ID | HGNC:11634 |
| Previous symbols | |
| Inheritance | |
| OMIM | 602272 |
| Chromosome | 18q21.2 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly |