Canonical Allele Identifier: PA211045
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 95651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Trp960Arg
CA211044
NM_001194998.2:c.2878T>C
CA392343234
NM_001194998.2:c.2878T>A