Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904026G>ACA255024F8c.5878C>T (p.Arg1960Ter)
c.5773C>T (p.Arg1925Ter)
ClinVar dbSNP
Xg.154904026G>TCA10567927F8c.5878C>A (p.Arg1960=)
c.5773C>A (p.Arg1925=)
dbSNP ExAC gnomAD

Number of alleles fetched