Canonical Allele Identifier: PA2827709765
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_001340055.1:p.Thr181Ser
CA2628511
NM_001353126.2:c.542C>G
CA354629289
NM_001353126.2:c.541A>T