ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.38367356T>C
CA224467
OTC
c.143T>C (p.Phe48Ser)
c.172-298765T>C (n.172-298765T>C)
n.235T>C
ClinVar
dbSNP
gnomAD v4
X
g.38367356T=
CA2424870819
OTC
c.143T= (p.Phe48=)
c.172-298765T= (n.172-298765T=)
n.235T=
dbSNP
Number of alleles fetched
Previous
Next