Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.112913980C>TCA119998SLC16A1c.1414G>A (p.Gly472Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.112913980C=CA1140803096SLC16A1c.1414G= (p.Gly472=)
dbSNP
1g.112913980C>GCA341826827SLC16A1c.1414G>C (p.Gly472Arg)
dbSNP

Number of alleles fetched