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Browse result for Hemoglobin Val de Marne
※ introduction A Cornelia de Lange syndrome that has_material_basis_in heterozygous mutation in the SMC3 gene on chromosome 10q25.2.
Reference
DiseaseOntology: Hemoglobin Val de Marne
Reference
DiseaseOntology: Hemoglobin Val de Marne
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD05931 | P69905 | 30393 | HBA1; | Hemoglobin subunit alpha [Cleaved into: Hemopressin] | Homo sapiens |