Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226608T>CCA124787HBBc.284A>G (p.Asp95Gly)
n.216A>G
n.335A>G
c.*100A>G (n.*100A>G)
 ClinVar dbSNP
11g.5226608T=CA1949567603HBBc.284A= (p.Asp95=)
n.216A=
n.335A=
c.*100A= (n.*100A=)
 dbSNP

Number of alleles fetched