Protein Variants | Comment | Organism |
---|---|---|
additional information | piebaldism is an autosomal dominant genetic disorder that results from Gly664Arg mutations within the tyrosine kinase domain of the c-Kit protooncogene | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | P10721 | - |
- |
Synonyms | Comment | Organism |
---|---|---|
mast/stem cell growth factor receptor | - |
Homo sapiens |