Allele Registry

Canonical Allele Identifier: PA915971657

Gene: CEP164 HGNC NCBI

ClinVar RCV:

RCV000951546

RCV001701259

ClinVar Variation:

772097

HGVS (amino-acid)	Matching Registered Transcripts
NP_055771.4:p.Pro127Leu	CA6294413 NM_014956.5:c.380C>T