Canonical Allele Identifier: PA2826195761
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 2791255
ClinVar RCV Id: RCV003672364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.His986Pro
CA392343042
NM_001194998.2:c.2957A>C