First observation of a mutation (R192Q) in a weak KEL2 phenotype encoded by 575 G>A, ethnic origin: Austria.. Homo sapiens KEL gene for Kell blood group system, KEL(R192Q) allele, exons 1-19.
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https://www.ncbi.nlm.nih.gov/bioproject/PRJEB46130
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资源简介：
Standard serologic typing identified a weakened KEL:2 expression in a blood donor sample. Molecular characterization identified a c.575G>A change on a KEL*2 background.
创建时间：
2021-07-11
