Hemoglobinopathies, Hemoglobin Variants, Hemoglobin S, Sickle Cell Disease, Hemoglobin C Disease, Hemoglobin E Disease, Thalassemia, Hemoglobin Barts, and Hereditary are other names for abnormal hemoglobins.
Two genes that code for hemoglobin "S" are inherited by people with this kind of SCD, one from each parent. The aberrant form of hemoglobin known as hemoglobin S makes red blood cells stiff and sickle-shaped. This condition, often known as sickle cell anemia, is typically the most serious one.
Atypical hemoglobin comes in more than 350 different varieties. Hemoglobin S is the most typical. Sickle cell illness results in the presence of this kind of hemoglobin.
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