Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.137234634C>TCA5364871SLC34A3c.1238C>T (p.Ala413Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.137234634C>ACA115010SLC34A3c.1238C>A (p.Ala413Glu)
 ClinVar dbSNP

Number of alleles fetched