| Approved symbol | INF2 |
|---|---|
| Approved name | inverted formin 2 |
| HGCN ID | HGNC:23791 |
| Previous symbols | C14orf151, C14orf173 |
| Inheritance | |
| OMIM | 610982 |
| Chromosome | 14q32.33 |
| Panel(s) |
NGS Mendelioom NGS Neuropathy/Charcot Marie Tooth |
| Approved symbol | INF2 |
|---|---|
| Approved name | inverted formin 2 |
| HGCN ID | HGNC:23791 |
| Previous symbols | C14orf151, C14orf173 |
| Inheritance | |
| OMIM | 610982 |
| Chromosome | 14q32.33 |
| Panel(s) |
NGS Mendelioom NGS Neuropathy/Charcot Marie Tooth |