Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904401C>TCA255182F8c.5710G>A (p.Glu1904Lys)
c.5605G>A (p.Glu1869Lys)
 ClinVar dbSNP
Xg.154904401C=CA2466828284F8c.5710G= (p.Glu1904=)
c.5605G= (p.Glu1869=)
 dbSNP

Number of alleles fetched