Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102066387C>TCA259880HPS6c.913C>T (p.Gln305Ter)
ClinVar dbSNP gnomAD v4
10g.102066387C=CA1932502983HPS6c.913C= (p.Gln305=)
dbSNP

Number of alleles fetched