Canonical Allele Identifier: PA2826434416
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 957287
ClinVar RCV Id: RCV001230240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244088.1:p.Gly264Ser
CA4485396
NM_001257159.2:c.790G>A