Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561829T>CCA255396F9c.1144T>C (p.Cys382Arg)
n.1723+88T>C
c.1030T>C (p.Cys344Arg)
c.1015T>C (p.Cys339Arg)
ClinVar dbSNP
Xg.139561829T>ACA336143348F9c.1144T>A (p.Cys382Ser)
n.1723+88T>A
c.1030T>A (p.Cys344Ser)
c.1015T>A (p.Cys339Ser)
ClinVar dbSNP

Number of alleles fetched