Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226997T>CCA125050HBBc.25A>G (p.Lys9Glu)
n.76A>G
ClinVar dbSNP
11g.5226997T>GCA124959HBBc.25A>C (p.Lys9Gln)
n.76A>C
ClinVar dbSNP
11g.5226997T=CA1949570983HBBc.25A= (p.Lys9=)
n.76A=
dbSNP

Number of alleles fetched