Canonical Allele Identifier: PA211088
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 158270
ClinVar RCV Id: RCV000145643 RCV000323485 RCV000380416 RCV000897088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Pro1693Leu
CA211086
NM_001194998.2:c.5078C>T