FORS > GBGT1*02N
Allele Information
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Phenotypes
FORS1
Genetic Changes
| nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
|---|---|---|---|---|---|---|---|
| c.363C>A | Exon 7 |
|
chr9:136,029,645 | chr9:133,154,258 |
 |
Sequence
None
Publication
None