Canonical Allele Identifier: PA645413995
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 434745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079456.2:p.Arg191Gln
CA2628433
NM_025180.5:c.572G>A