Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.40072420G>ACA255609BCORc.2926C>T (p.Arg976Ter)
n.2966C>T
c.1147C>T (p.Arg383Ter)
 ClinVar dbSNP COSMIC
Xg.40072420G=CA2425444207BCORc.2926C= (p.Arg976=)
n.2966C=
c.1147C= (p.Arg383=)
 dbSNP

Number of alleles fetched