Canonical Allele Identifier: PA658832887
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 546753
ClinVar RCV Id: RCV000658714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Ala956Val
CA7548455
NM_001194998.2:c.2867C>T