Canonical Allele Identifier: PA2826882023
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 3143108
ClinVar RCV Id: RCV004428477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Gly756Val
CA353882129
NM_001303401.2:c.2267G>T