ABO > ABO*BW.02
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Phenotypes
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A,B
A1
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.873C>G p.Asp291Glu Exon 7 chr9:136,131,245 chr9:133,255,829
 
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