Canonical Allele Identifier: PA2826881867
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2061223
ClinVar RCV Id: RCV002942561 RCV004067258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.His39Gln
CA2521802
NM_001303401.2:c.117C>G
CA353883996
NM_001303401.2:c.117C>A