H > FUT1*01N.21
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.13_19dup Exon 4 chr19:49,254,526 chr19:48,751,269
 
 
 
 
 
 
 
 
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