Canonical Allele Identifier: PA2827709671
Gene: CEP63 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340054.1:p.Ser183Gly
CA354627518
NM_001353125.2:c.547A>G