Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.1406226G>ACA149716SLC6A3c.1561C>T (p.Arg521Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
5g.1406226G>TCA443019689SLC6A3c.1561C>A (p.Arg521=)
dbSNP gnomAD v4
5g.1406226G=CA1522618902SLC6A3c.1561C= (p.Arg521=)
dbSNP

Number of alleles fetched