Canonical Allele Identifier: PA211042
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 158247
ClinVar RCV Id: RCV000145618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Glu943Lys
CA211041
NM_001194998.2:c.2827G>A