Canonical Allele Identifier: PA2825399622
Gene: CEP63 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035859.1:p.Arg46His
CA2628269
NM_001042400.3:c.137G>A