I > GCNT2*01W.02
Allele Information
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Phenotypes
I
Genetic Changes
| nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
|---|---|---|---|---|---|---|---|
| c.505G>A | p.Ala169Thr | Exon 1 |
|
chr6:10,586,727 | chr6:10,586,494 |
 |
Sequence
None
Publication
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