Allele Registry

Canonical Allele Identifier: PA916035712

Gene: CEP63 HGNC NCBI

ClinVar RCV:

RCV000331060

ClinVar Variation:

287199

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340047.1:p.Thr311Ser	CA2628511 NM_001353118.1:c.932C>G CA354629289 NM_001353118.1:c.931A>T