ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.70027937C>A
CA413448337
EDA
c.607C>A (p.Pro203Thr)
c.211C>A (p.Pro71Thr)
ClinVar
dbSNP
gnomAD v4
X
g.70027937C>T
CA261501
EDA
c.607C>T (p.Pro203Ser)
c.211C>T (p.Pro71Ser)
ClinVar
dbSNP
Number of alleles fetched
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