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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.47447853G>A
CA119256
RAPSN
c.490C>T (p.Arg164Cys)
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
COSMIC
11
g.47447853G>C
CA380333737
RAPSN
c.490C>G (p.Arg164Gly)
ClinVar
dbSNP
Number of alleles fetched
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