About this document
Hemoglobin Mutation and Sickle Cell Anemia by 2401600199 is a document available to read on EtoBox.
The document is an assignment on bioinformatics focusing on the hemoglobin β chain and its mutation leading to Sickle Cell Anemia. It details the specific mutation where glutamic acid is replaced by valine due to a single point mutation in the β-globin gene. The document also includes wild type and mutant sequences along with their E value and percentage identity.
- Author
- 2401600199
- Language
- EN