Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154903966G>ACA255190F8c.5938C>T (p.His1980Tyr)
c.5833C>T (p.His1945Tyr)
 ClinVar dbSNP
Xg.154903966G>CCA414905825F8c.5938C>G (p.His1980Asp)
c.5833C>G (p.His1945Asp)
 dbSNP

Number of alleles fetched