Canonical Allele Identifier: PA2827709000
Gene: CEP63 HGNC NCBI
ClinVar RCV:
RCV001907021
ClinVar Variation:
1406907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340048.1:p.Ala264Ser
CA354628972
NM_001353119.2:c.790G>T