Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225647T>GCA125158HBBc.395A>C (p.Gln132Pro)
c.*211A>C (n.*211A>C)
 ClinVar dbSNP
11g.5225647T>CCA125391HBBc.395A>G (p.Gln132Arg)
c.*211A>G (n.*211A>G)
 ClinVar dbSNP

Number of alleles fetched