Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142181T>ACA020273VHLc.334T>A (p.Tyr112Asn)
 ClinVar dbSNP
3g.10142181T>CCA020277VHLc.334T>C (p.Tyr112His)
 ClinVar dbSNP

Number of alleles fetched