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
The authors have disclosed no conflicts of interest. The data that support the findings of this study are openly available in NCBI GenBank at https://www.ncbi.nlm.nih.gov/genbank/, reference number PX627881.