Canonical Allele Identifier: PA658680137
Gene: CEP104 HGNC NCBI

Linked Data

ClinVar Variation Id: 475462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055519.1:p.Ala882Ser
CA551219
NM_014704.3:c.2644G>T