H > FUT1*01W.22
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.991C>A p.Pro331Thr Exon 4 chr19:49,253,548 chr19:48,750,291
 
 
 
 
 
 
 
 
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