| Approved symbol | FOXA2 |
|---|---|
| Approved name | forkhead box A2 |
| HGCN ID | HGNC:5022 |
| Previous symbols | HNF3B |
| Inheritance | |
| OMIM | 600288 |
| Chromosome | 20p11.21 |
| Panel(s) |
NGS Hyperinsulinisme NGS Hypothyreodie NGS Mendelioom |
| Approved symbol | FOXA2 |
|---|---|
| Approved name | forkhead box A2 |
| HGCN ID | HGNC:5022 |
| Previous symbols | HNF3B |
| Inheritance | |
| OMIM | 600288 |
| Chromosome | 20p11.21 |
| Panel(s) |
NGS Hyperinsulinisme NGS Hypothyreodie NGS Mendelioom |