Allele Registry

Canonical Allele Identifier: PA645485129

Gene: CEP41 HGNC NCBI

ClinVar Variation Id: 235611

HGVS (amino-acid)	Matching Registered Transcripts
NP_061188.1:p.Ala107Gly	CA4485603 NM_018718.3:c.320C>G