Canonical Allele Identifier: PA1139727954
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_061188.1:p.Gly352Ser
CA4485396
NM_018718.3:c.1054G>A