Canonical Allele Identifier: PA2827709370
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406907
ClinVar RCV Id: RCV001907021
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340051.1:p.Ala264Ser
CA354628972
NM_001353122.1:c.790G>T