Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.137233722G>ACA115012SLC34A3c.846G>A (p.Pro282=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.137233722G=CA1884370671SLC34A3c.846G= (p.Pro282=)
dbSNP
9g.137233722G>TCA467868150SLC34A3c.846G>T (p.Pro282=)
ClinVar dbSNP

Number of alleles fetched