Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904025C>TCA255019F8c.5879G>A (p.Arg1960Gln)
c.5774G>A (p.Arg1925Gln)
 ClinVar dbSNP
Xg.154904025C>ACA255185F8c.5879G>T (p.Arg1960Leu)
c.5774G>T (p.Arg1925Leu)
 ClinVar dbSNP

Number of alleles fetched