Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142173T>ACA020268VHLc.326T>A (p.Ile109Asn)
ClinVar dbSNP
3g.10142173T>CCA351751268VHLc.326T>C (p.Ile109Thr)
ClinVar dbSNP
3g.10142173T=CA1345066497VHLc.326T= (p.Ile109=)
dbSNP

Number of alleles fetched