Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225708C>GCA037014HBBc.334G>C (p.Val112Leu)
n.266G>C
c.*150G>C (n.*150G>C)
 ClinVar dbSNP
11g.5225708C>ACA125098HBBc.334G>T (p.Val112Phe)
n.266G>T
c.*150G>T (n.*150G>T)
 ClinVar dbSNP

Number of alleles fetched