Allele Registry

Canonical Allele Identifier: PA2827709668

Gene: CEP63 HGNC NCBI

ClinVar RCV:

RCV000501571

RCV000948660

ClinVar Variation:

434745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340054.1:p.Arg163Gln	CA2628433 NM_001353125.2:c.488G>A