Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154957079C>TCA255111F8c.1630G>A (p.Asp544Asn)
c.*1506G>A (n.*1506G>A)
c.1525G>A (p.Asp509Asn)
 ClinVar dbSNP
Xg.154957079C=CA2466845353F8c.1630G= (p.Asp544=)
c.*1506G= (n.*1506G=)
c.1525G= (p.Asp509=)
 dbSNP

Number of alleles fetched