Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56870119C>TCA119768SLC12A3c.625C>T (p.Arg209Trp)
c.622C>T (p.Arg208Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.56870119C=CA2224349275SLC12A3c.625C= (p.Arg209=)
c.622C= (p.Arg208=)
 dbSNP

Number of alleles fetched