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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
5
g.78969095C>T
CA3318273
ARSB
c.410G>A (p.Gly137Asp)
n.481G>A
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v4
5
g.78969095C>A
CA114600
ARSB
c.410G>T (p.Gly137Val)
n.481G>T
ClinVar
dbSNP
gnomAD v4
Number of alleles fetched
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