Canonical Allele Identifier: PA645407286
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 285113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055771.4:p.Arg480Trp
CA6294759
NM_014956.5:c.1438C>T