Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.103565295G>TCA154902RELNc.5193C>A (p.Tyr1731Ter)
n.5077C>A
n.2896C>A
 ClinVar dbSNP gnomAD v4
7g.103565295G=CA1730791645RELNc.5193C= (p.Tyr1731=)
n.5077C=
n.2896C=
 dbSNP

Number of alleles fetched