Canonical Allele Identifier: PA645407236
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 421579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055771.4:p.Pro127His
CA6294412
NM_014956.5:c.380C>A