ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA915971657
Gene: CEP164
HGNC
NCBI
Linked Data
ClinVar Variation Id:
772097
ClinVar RCV Id:
RCV000951546
RCV001701259
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_055771.4:p.Pro127Leu
CA6294413
NM_014956.5:c.380C>T