Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.46115882G>TCA410524658COL6A2c.812G>T (p.Gly271Val)
n.468G>T
n.935G>T
n.942G>T
 ClinVar dbSNP
21g.46115882G>ACA275346COL6A2c.812G>A (p.Gly271Asp)
n.468G>A
n.935G>A
n.942G>A
 ClinVar dbSNP

Number of alleles fetched