ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.100407902A>C
CA414008610
PCDH19
c.696T>G (p.Asn232Lys)
ClinVar
dbSNP
X
g.100407902A>T
CA316321
PCDH19
c.696T>A (p.Asn232Lys)
ClinVar
dbSNP
Number of alleles fetched
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