Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.45989626G>CCA410521779COL6A1c.877G>C (p.Gly293Arg)
 ClinVar dbSNP
21g.45989626G>ACA221801COL6A1c.877G>A (p.Gly293Arg)
 ClinVar dbSNP

Number of alleles fetched