Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225704C>TCA125364HBBc.338G>A (p.Cys113Tyr)
n.270G>A
c.*154G>A (n.*154G>A)
 ClinVar dbSNP
11g.5225704C>ACA125505HBBc.338G>T (p.Cys113Phe)
n.270G>T
c.*154G>T (n.*154G>T)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched