Allele Registry

Canonical Allele Identifier: PA645485149

Gene: CEP41 HGNC NCBI

ClinVar Allele:

301934

ClinVar RCV:

RCV000441831

RCV001087358

RCV003922589

ClinVar Variation:

358939

HGVS (amino-acid)	Matching Registered Transcripts
NP_061188.1:p.Ser337Pro	CA4485409 NM_018718.3:c.1009T>C