Canonical Allele Identifier: PA645484756
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Ile1392Thr
CA7548145
NM_001194998.2:c.4175T>C