Canonical Allele Identifier: PA2830028199
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1973555
ClinVar RCV Id: RCV002750579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079456.2:p.Ser211Gly
CA354627518
NM_025180.5:c.631A>G