Canonical Allele Identifier: PA2826881947
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2995734
ClinVar RCV Id: RCV003853821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Ile434Val
CA2522136
NM_001303401.2:c.1300A>G