Canonical Allele Identifier: PA2826195740
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423741
ClinVar RCV Id: RCV001954885 RCV002561341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Glu943Gly
CA7548467
NM_001194998.2:c.2828A>G