Canonical Allele Identifier: PA2827707755
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1905196
ClinVar RCV Id: RCV002592881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340039.1:p.Arg46His
CA2628269
NM_001353110.1:c.137G>A