Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.50197009C>TCA400223631COL1A1c.804+1G>A (n.804+1G>A)
n.531+1G>A
ClinVar dbSNP
17g.50197009C>GCA16043534COL1A1c.804+1G>C (n.804+1G>C)
n.531+1G>C
ClinVar dbSNP

Number of alleles fetched