Canonical Allele Identifier: PA2580462371
Gene: CEP97 HGNC NCBI
ClinVar RCV:
RCV002581365
ClinVar Variation:
1908189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Ala178Thr
CA79787228
NM_024548.4:c.532G>A