Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.7690059A>CCA16619590GDF3c.914T>G (p.Leu305Arg)
ClinVar dbSNP
12g.7690059A>GCA129364GDF3c.914T>C (p.Leu305Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched