ABO > ABO*A3.01
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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.871G>A p.Asp291Asn Exon 7 chr9:136,131,247 chr9:133,255,831
 
 
 
 
 
 
 
 
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