Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.43731695G>TCA163205MAOAc.398G>T (p.Cys133Phe)
c.107G>T (p.Cys36Phe)
n.929G>T
n.353G>T
c.692G>T (p.Cys231Phe)
c.797G>T (p.Cys266Phe)
ClinVar dbSNP
Xg.43731695G=CA2426670049MAOAc.398G= (p.Cys133=)
c.107G= (p.Cys36=)
n.929G=
n.353G=
c.692G= (p.Cys231=)
c.797G= (p.Cys266=)
dbSNP

Number of alleles fetched