H > FUT1*01N.11
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.785G>A Exon 4 chr19:49,253,754 chr19:48,750,497
 
c.786C>A Exon 4 chr19:49,253,753 chr19:48,750,496
 
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