Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154966671A>TCA255087F8c.1026T>A (p.Tyr342Ter)
c.*902T>A (n.*902T>A)
c.921T>A (p.Tyr307Ter)
 ClinVar dbSNP
Xg.154966671A=CA2466848168F8c.1026T= (p.Tyr342=)
c.*902T= (n.*902T=)
c.921T= (p.Tyr307=)
 dbSNP

Number of alleles fetched