Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.70033426G>ACA273144EDAc.822G>A (p.Trp274Ter)
c.813G>A (p.Trp271Ter)
c.426G>A (p.Trp142Ter)
 ClinVar dbSNP
Xg.70033426G>TCA261505EDAc.822G>T (p.Trp274Cys)
c.813G>T (p.Trp271Cys)
c.426G>T (p.Trp142Cys)
 ClinVar dbSNP

Number of alleles fetched