Canonical Allele Identifier: PA2827708800
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 287199
ClinVar RCV Id: RCV000331060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340046.1:p.Thr302Ser
CA2628511
NM_001353117.2:c.905C>G
CA354629289
NM_001353117.2:c.904A>T