Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225707A>GCA125176HBBc.335T>C (p.Val112Ala)
n.267T>C
c.*151T>C (n.*151T>C)
 ClinVar dbSNP gnomAD v4
11g.5225707A=CA1949565164HBBc.335T= (p.Val112=)
n.267T=
c.*151T= (n.*151T=)
 dbSNP

Number of alleles fetched