Canonical Allele Identifier: PA658810364
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 521386
ClinVar RCV Id: RCV000624521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.His969Tyr
CA7548448
NM_014985.4:c.2905C>T