Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226605T>ACA124945HBBc.287A>T (p.Lys96Met)
n.219A>T
n.338A>T
c.*103A>T (n.*103A>T)
 ClinVar dbSNP
11g.5226605T=CA1949567581HBBc.287A= (p.Lys96=)
n.219A=
n.338A=
c.*103A= (n.*103A=)
 dbSNP

Number of alleles fetched