Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225627C>GCA124766HBBc.415G>C (p.Ala139Pro)
c.*231G>C (n.*231G>C)
 ClinVar dbSNP
11g.5225627C>TCA125521HBBc.415G>A (p.Ala139Thr)
c.*231G>A (n.*231G>A)
 ClinVar dbSNP

Number of alleles fetched