Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139562009G>ACA255418F9c.1324G>A (p.Gly442Arg)
n.1723+268G>A
c.1210G>A (p.Gly404Arg)
c.1195G>A (p.Gly399Arg)
 ClinVar dbSNP COSMIC
Xg.139562009G=CA2461412292F9c.1324G= (p.Gly442=)
n.1723+268G=
c.1210G= (p.Gly404=)
c.1195G= (p.Gly399=)
 dbSNP

Number of alleles fetched