ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826541909
Gene: CEP164
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1328075
ClinVar RCV Id:
RCV001795509
RCV001795510
RCV002544330
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001258862.1:p.Gln27Lys
CA229370653
NM_001271933.2:c.79C>A