Canonical Allele Identifier: PA645484784
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 434735
ClinVar RCV Id: RCV000501448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Leu1568Ile
CA392333845
NM_001194998.2:c.4702C>A