Canonical Allele Identifier: PA2826195743
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150223
ClinVar RCV Id: RCV003071821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Val948Leu
CA7548463
NM_001194998.2:c.2842G>C