Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.35037010C>TCA3229361AGXT2c.418G>A (p.Val140Ile)
n.327G>A
c.415G>A (p.Val139Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.35037010C>ACA359421044AGXT2c.418G>T (p.Val140Phe)
n.327G>T
c.415G>T (p.Val139Phe)
 dbSNP

Number of alleles fetched