Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561565C>ACA518916374F9c.880C>A (p.Arg294=)
n.1547C>A
c.766C>A (p.Arg256=)
c.751C>A (p.Arg251=)
 dbSNP gnomAD v2
Xg.139561565C>TCA255344F9c.880C>T (p.Arg294Ter)
n.1547C>T
c.766C>T (p.Arg256Ter)
c.751C>T (p.Arg251Ter)
 ClinVar dbSNP

Number of alleles fetched