Canonical Allele Identifier: PA211073
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 158262
ClinVar RCV Id: RCV000145634 RCV000270516 RCV000381261 RCV000969294 RCV004532649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Gln1358Glu
CA211071
NM_001194998.2:c.4072C>G