Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225621C>TCA125141HBBc.421G>A (p.Ala141Thr)
c.*237G>A (n.*237G>A)
 ClinVar dbSNP
11g.5225621C=CA1949564313HBBc.421G= (p.Ala141=)
c.*237G= (n.*237G=)
 dbSNP

Number of alleles fetched