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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
21
g.45990792G>A
CA257736
COL6A1
c.1022G>A (p.Gly341Asp)
ClinVar
dbSNP
COSMIC
21
g.45990792G>T
CA10604208
COL6A1
c.1022G>T (p.Gly341Val)
ClinVar
dbSNP
Number of alleles fetched
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