Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.66863791G>ACA339942PCc.1351C>T (p.Arg451Cys)
n.290-13726C>T
c.1231C>T (p.Arg411Cys)
 ClinVar dbSNP gnomAD v4
11g.66863791G=CA1979886647PCc.1351C= (p.Arg451=)
n.290-13726C=
c.1231C= (p.Arg411=)
 dbSNP

Number of alleles fetched