Canonical Allele Identifier: PA2827708744
Gene: CEP63 HGNC NCBI
ClinVar RCV:
RCV002592881
ClinVar Variation:
1905196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340046.1:p.Arg46His
CA2628269
NM_001353117.2:c.137G>A