7uzq
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Local refinement of RhAG-RhCE-ANK1(AR1-5), from consensus refinement of all classes
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Structural highlights
DiseaseRHCE_HUMAN Rh deficiency syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionRHCE_HUMAN May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane. See Also | ||||||||||||||||||||
This page was last modified 09:39, 14 February 2024.