Canonical Allele Identifier: PA2827707806
Gene: CEP63 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340039.1:p.Ala264Ser
CA354628972
NM_001353110.1:c.790G>T