Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.65537671T>ACA501691219AXIN2c.1365A>T (p.Pro455=)
c.397-8971A>T (n.397-8971A>T)
ClinVar dbSNP gnomAD v4
17g.65537671T>CCA8718672AXIN2c.1365A>G (p.Pro455=)
c.397-8971A>G (n.397-8971A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched