Hemoglobin E - beta-thalassemia

Hemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain. At position 26 there is a change in the amino acid, from glutamic acid to lysine (E26K). [Source: Wikipedia ]

Synonyms
E - beta-thalassemia
HbE - beta-thalassemia
OrphaNet reference
Hemoglobin E - beta-thalassemia 
May Cause
Beta-thalassemia
Hemoglobin E