Canonical Allele Identifier: PA2826195526
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Asn321Ser
CA7548987
NM_001194998.2:c.962A>G