Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969354C>ACA414917650F8c.986G>T (p.Cys329Phe)
c.*862G>T (n.*862G>T)
c.881G>T (p.Cys294Phe)
 dbSNP
Xg.154969354C>TCA255089F8c.986G>A (p.Cys329Tyr)
c.*862G>A (n.*862G>A)
c.881G>A (p.Cys294Tyr)
 ClinVar dbSNP

Number of alleles fetched