Canonical Allele Identifier: PA2827342579
Gene: CEP78 HGNC NCBI

Linked Data

ClinVar Variation Id: 1959405
ClinVar RCV Id: RCV002701260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317620.1:p.Ser300Ala
CA373856514
NM_001330691.3:c.898T>G