Canonical Allele Identifier: PA2827708871
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 434745
ClinVar RCV Id: RCV000501571 RCV000948660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340047.1:p.Arg200Gln
CA2628433
NM_001353118.1:c.599G>A