Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969468T>CCA255017F8c.872A>G (p.Glu291Gly)
c.*748A>G (n.*748A>G)
c.767A>G (p.Glu256Gly)
 ClinVar dbSNP
Xg.154969468T=CA2466849027F8c.872A= (p.Glu291=)
c.*748A= (n.*748A=)
c.767A= (p.Glu256=)
 dbSNP

Number of alleles fetched