Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.46115873G>ACA215992COL6A2c.803G>A (p.Gly268Asp)
n.459G>A
n.926G>A
n.933G>A
 ClinVar dbSNP
21g.46115873G>TCA410524590COL6A2c.803G>T (p.Gly268Val)
n.459G>T
n.926G>T
n.933G>T
 ClinVar dbSNP

Number of alleles fetched