Human hemoglobin includes two alpha and two beta chains to produce a heterotetramer. In Sickle Mobile Anemia, the sixth codon of the beta chain is made up of a missense mutation, where glutamic acid, a billed amino acid, is changed with valine, a neutral amino acid. Due to this fact, https://finnbhnsx.signalwiki.com/419933/helping_the_others_realize_the_advantages_of_recombinant_protein_production