Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142133C>TCA351750811VHLc.286C>T (p.Gln96Ter)
ClinVar dbSNP COSMIC
3g.10142133C=CA1345066200VHLc.286C= (p.Gln96=)
dbSNP

Number of alleles fetched