CVT15 Summary 
| Standard Name | CVT15 |
|---|---|
| Feature Type | not physically mapped |
Mutant phenotypes All CVT15 Phenotype evidence and references
| Classical genetics | |
|---|---|
| reduction of function |
Resources
| External Links | Search all NCBI (Entrez) |
|---|
| Primary SGDID | S000029128 |
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