Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226988C>ACA125412HBBc.34G>T (p.Val12Phe)
n.85G>T
ClinVar dbSNP
11g.5226988C>TCA124888HBBc.34G>A (p.Val12Ile)
n.85G>A
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched