H > FUT1*01N.17
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.1047G>C p.Trp349Cys Exon 4 chr19:49,253,492 chr19:48,750,235
 
 
 
 
 
 
 
 
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