H > FUT1*02W.04
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Phenotypes
H
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.980A>C p.Asn327Thr Exon 4 chr19:49,253,559 chr19:48,750,302
 
 
 
 
 
 
 
 
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