Canonical Allele Identifier: PA915982451
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 235611
ClinVar RCV Id: RCV000224397 RCV000265231 RCV001261713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244088.1:p.Ala91Gly
CA4485603
NM_001257159.2:c.272C>G