Genomics

Dataset Information

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Homo sapiens KEL gene for Kell blood group system, KEL(R192Q) allele, exons 1-19.


ABSTRACT: First observation of a mutation (R192Q) in a weak KEL2 phenotype encoded by 575 G>A, ethnic origin: Austria.

PROVIDER: PRJEB46130 | ENA |

REPOSITORIES: ENA

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