H > FUT1*01W.05.01
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.460T>C p.Tyr154His Exon 4 chr19:49,254,079 chr19:48,750,822
 
 
 
 
 
 
 
 
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