Canonical Allele Identifier: PA2830010604
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 3143108
ClinVar RCV Id: RCV004428477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Gly815Val
CA353882129
NM_024548.4:c.2444G>T