Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5248400C>TCA124624HBG1,HBG2c.403G>A (p.Val135Met)
c.466G>A (p.Val156Met)
n.1334G>A
 ClinVar dbSNP COSMIC
11g.5248400C=CA1949582155HBG1,HBG2c.403G= (p.Val135=)
c.466G= (p.Val156=)
n.1334G=
 dbSNP

Number of alleles fetched