Canonical Allele Identifier: PA2827709760
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_001340055.1:p.Ala143Ser
CA354628972
NM_001353126.2:c.427G>T