Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154899876G>ACA255200F8c.6263C>T (p.Ser2088Phe)
c.6158C>T (p.Ser2053Phe)
 ClinVar dbSNP
Xg.154899876G>TCA414902765F8c.6263C>A (p.Ser2088Tyr)
c.6158C>A (p.Ser2053Tyr)
 dbSNP

Number of alleles fetched