Canonical Allele Identifier: PA645485149
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 358939
ClinVar RCV Id: RCV000441831 RCV001087358 RCV003922589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061188.1:p.Ser337Pro
CA4485409
NM_018718.3:c.1009T>C