Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226990G>TCA124726HBBc.32C>A (p.Ala11Asp)
n.83C>A
 ClinVar dbSNP
11g.5226990G>ACA125466HBBc.32C>T (p.Ala11Val)
n.83C>T
 ClinVar dbSNP gnomAD v4

Number of alleles fetched