Canonical Allele Identifier: PA2827707790
Gene: CEP63 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340039.1:p.Ser211Gly
CA354627518
NM_001353110.1:c.631A>G