IN > IN*02.-04
Allele Information
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Phenotypes
Ina
Inb
INFI
INJA
INRA
INSL
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.488C>A Exon 5 chr11:35,211,433 chr11:35,189,886
 
 
 
 
 
 
 
 
Sequence
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