Protein Variants | Comment | Organism |
---|---|---|
Q446H | the mutation is associated with the occurrence of congenital hypothyroidism | Homo sapiens |
W527C | the mutation is associated with the occurrence of congenital hypothyroidism | Homo sapiens |
W873X | the mutation is associated with the occurrence of congenital hypothyroidism | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|
Synonyms | Comment | Organism |
---|---|---|
thyroid peroxidase | - |
Homo sapiens |
TPO | - |
Homo sapiens |