Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.121307244G>ACA118736SC5Dc.632G>A (p.Gly211Asp)
n.925G>A
n.325G>A
c.631+1G>A (n.631+1G>A)
 ClinVar dbSNP
11g.121307244G=CA2004810545SC5Dc.632G= (p.Gly211=)
n.925G=
n.325G=
c.631+1G= (n.631+1G=)
 dbSNP

Number of alleles fetched