Canonical Allele Identifier: PA2580407296
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920652
ClinVar RCV Id: RCV002621130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061188.1:p.Asp322Gly
CA369286908
NM_018718.3:c.965A>G