Canonical Allele Identifier: PA2826881945
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2359169
ClinVar RCV Id: RCV004200880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Ile430Thr
CA2522133
NM_001303401.2:c.1289T>C