I > GCNT2*01N.05
Allele Information
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Phenotypes
I
Genetic Changes
nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
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c.984G>A | p.Trp328* | Exon 2 | chr6:10,621,642 | chr6:10,621,409 |
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Sequence
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