Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.45989617G>ACA221800COL6A1c.868G>A (p.Gly290Arg)
 ClinVar dbSNP COSMIC
21g.45989617G>TCA410521749COL6A1c.868G>T (p.Gly290Trp)
 ClinVar dbSNP
21g.45989617G>CCA127117COL6A1c.868G>C (p.Gly290Arg)
 ClinVar dbSNP

Number of alleles fetched