Allele Registry

Canonical Allele Identifier: PA2826541896

Gene: CEP164 HGNC NCBI

ClinVar RCV:

RCV001369702

RCV004037091

ClinVar Variation:

1060292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258862.1:p.Pro5Thr	CA6294295 NM_001271933.2:c.13C>A