Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904989G>ACA414908976F8c.5408C>T (p.Ser1803Phe)
c.5303C>T (p.Ser1768Phe)
 dbSNP
Xg.154904989G>TCA255165F8c.5408C>A (p.Ser1803Tyr)
c.5303C>A (p.Ser1768Tyr)
 ClinVar dbSNP

Number of alleles fetched