Canonical Allele Identifier: PA915971657
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 772097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055771.4:p.Pro127Leu
CA6294413
NM_014956.5:c.380C>T