Canonical Allele Identifier: PA2827709692
Gene: CEP63 HGNC NCBI
ClinVar RCV:
RCV000331060
ClinVar Variation:
287199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340054.1:p.Thr274Ser
CA2628511
NM_001353125.2:c.821C>G
CA354629289
NM_001353125.2:c.820A>T