ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826195756
Gene: CEP152
HGNC
NCBI
Linked Data
ClinVar Variation Id:
885097
ClinVar RCV Id:
RCV001116507
RCV001116506
RCV002558153
RCV002556464
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001181927.1:p.Arg980Gln
CA269537959
NM_001194998.2:c.2939G>A