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Browse result for Hemoglobin Harbin

※ introduction

    An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other.

Reference
DiseaseOntology: Hemoglobin Harbin


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD05931P6990530393
HBA1;
Hemoglobin subunit alpha [Cleaved into: Hemopressin]
Homo sapiens