Allele Registry

Canonical Allele Identifier: PA2826434212

Gene: CEP41 HGNC NCBI

ClinVar Allele:

301936

ClinVar RCV:

RCV000483238

RCV000878420

RCV001261666

RCV001702359

RCV003922590

ClinVar Variation:

358942

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244087.1:p.Pro206Ala	CA4485523 NM_001257158.2:c.616C>G