H > FUT1*01N.13
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.881_882delTT p.Phe294Cysfs*40 Exon 4 chr19:49,253,658 chr19:48,750,401
 
 
 
 
 
 
 
 
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