Canonical Allele Identifier: PA2827709483
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 377098
ClinVar RCV Id: RCV000439538 RCV000500958 RCV001270066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340052.1:p.Asn223Ser
CA2628451
NM_001353123.2:c.668A>G