Canonical Allele Identifier: PA2826434248
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 358940
ClinVar RCV Id: RCV000794924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244087.1:p.Arg263Lys
CA4485410
NM_001257158.2:c.788G>A