Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele

Key Points

• The study aims to identify and describe a novel nonsense variant within the ABO*B.01 allele.
• Data collected from NCBI GenBank
• Reference number provided for data access
• Identification of variant c.184C>T
• Novel allele variation reported
• Data made publicly available for further analysis

Abstract