Canonical Allele Identifier: PA2826881891
Gene: CEP97 HGNC NCBI
ClinVar RCV:
RCV002867493
ClinVar Variation:
2031808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Asp184Asn
CA353886382
NM_001303401.2:c.550G>A