Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969438C>TCA255079F8c.902G>A (p.Arg301His)
c.*778G>A (n.*778G>A)
c.797G>A (p.Arg266His)
 ClinVar dbSNP
Xg.154969438C>ACA255080F8c.902G>T (p.Arg301Leu)
c.*778G>T (n.*778G>T)
c.797G>T (p.Arg266Leu)
 ClinVar dbSNP

Number of alleles fetched