G2Cdb::Allele report
- Mutation type
- MI
Altered genes (1)
Gene |
Symbol |
Species |
Description |
G00001453 |
PTPN11 |
Homo sapiens |
protein tyrosine phosphatase, non-receptor type 11 |
Diseases (1)
Disease |
Description |
Nervous effect |
D00000305 |
Noonan syndrome |
N |
Literature (1)
Pubmed - human_disease