Allele Registry

Canonical Allele Identifier: PA2826434403

Gene: CEP41 HGNC NCBI

ClinVar Allele:

301934

ClinVar RCV:

RCV000441831

RCV001087358

RCV003922589

ClinVar Variation:

358939

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244088.1:p.Ser249Pro	CA4485409 NM_001257159.2:c.745T>C