Canonical Allele Identifier: PA2826195745
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 1329817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Lys955Met
CA7548457
NM_001194998.2:c.2864A>T