Canonical Allele Identifier: PA2826195751
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 521386
ClinVar RCV Id: RCV000624521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.His969Tyr
CA7548448
NM_001194998.2:c.2905C>T