Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154966525C>TCA120918F8c.1172G>A (p.Arg391His)
c.*1048G>A (n.*1048G>A)
c.1067G>A (p.Arg356His)
 ClinVar dbSNP COSMIC COSMIC
Xg.154966525C>ACA414916367F8c.1172G>T (p.Arg391Leu)
c.*1048G>T (n.*1048G>T)
c.1067G>T (p.Arg356Leu)
 dbSNP

Number of alleles fetched