Canonical Allele Identifier: PA2826195518
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316429
ClinVar RCV Id: RCV000265493 RCV000320543 RCV000420504 RCV000965295 RCV002522801 RCV004537785
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Lys309Gln
CA7548993
NM_001194998.2:c.925A>C