Canonical Allele Identifier: PA2827707632
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 377098
ClinVar RCV Id: RCV000439538 RCV000500958 RCV001270066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340038.1:p.Asn223Ser
CA2628451
NM_001353109.1:c.668A>G