Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.120788801C>GCA251420TSPAN12c.709G>C (p.Ala237Pro)
c.688G>C (n.688G>C)
c.634G>C (p.Ala212Pro)
ClinVar dbSNP
7g.120788801C>TCA369133754TSPAN12c.709G>A (p.Ala237Thr)
c.688G>A (n.688G>A)
c.634G>A (p.Ala212Thr)
dbSNP

Number of alleles fetched