IN > IN*01 or IN*A
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.137G>C | Exon 2 | chr11:35,198,191 | chr11:35,176,644 |
Sequence
None
Publication
None