Allele Registry

Canonical Allele Identifier: PA2827374629

Gene: CEP83 HGNC NCBI

ClinVar Allele:

1048196

ClinVar RCV:

RCV001365769

ClinVar Variation:

1056876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333391.1:p.Met248Val	CA6721772 NM_001346462.2:c.742A>G