G2Cdb::Allele report
- Mutation type
- MI
Altered genes (1)
| Gene | Symbol | Species | Description |
|---|---|---|---|
| G00001881 | L1CAM | Homo sapiens | L1 cell adhesion molecule |
Diseases (1)
| Disease | Description | Nervous effect |
|---|---|---|
| D00000198 | Epilepsy (autosomal dominant partial with auditory features) | Y |