Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154928668G>ACA120919F8c.5122C>T (p.Arg1708Cys)
c.5017C>T (p.Arg1673Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.154928668G>TCA414913844F8c.5122C>A (p.Arg1708Ser)
c.5017C>A (p.Arg1673Ser)
 dbSNP

Number of alleles fetched