| Standard Name | CVT14 |
|---|---|
| Feature Type | not physically mapped |
Mutant phenotypes All CVT14 Phenotype evidence and references
| Classical genetics | |
|---|---|
| reduction of function |
Resources
| External Links | Search all NCBI (Entrez) |
|---|
| Primary SGDID | S000029127 |
|---|
| Standard Name | CVT14 |
|---|---|
| Feature Type | not physically mapped |
| Classical genetics | |
|---|---|
| reduction of function |
| External Links | Search all NCBI (Entrez) |
|---|
| Primary SGDID | S000029127 |
|---|