Canonical Allele Identifier: PA103709
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 30843
ClinVar RCV Id: RCV000023828 RCV001295978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061188.1:p.Arg360Cys
CA129496
NM_018718.3:c.1078C>T