Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154957027T>CCA255117F8c.1682A>G (p.Asp561Gly)
c.*1558A>G (n.*1558A>G)
c.1577A>G (p.Asp526Gly)
 ClinVar dbSNP
Xg.154957027T=CA2466845329F8c.1682A= (p.Asp561=)
c.*1558A= (n.*1558A=)
c.1577A= (p.Asp526=)
 dbSNP

Number of alleles fetched