Canonical Allele Identifier: PA2826195759
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 2550835
ClinVar RCV Id: RCV003258515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Asp984His
CA392343063
NM_001194998.2:c.2950G>C