Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.45990257G>CCA10606786COL6A1c.931-1G>C (n.931-1G>C)
ClinVar dbSNP
21g.45990257G>ACA10604117COL6A1c.931-1G>A (n.931-1G>A)
ClinVar dbSNP

Number of alleles fetched