Canonical Allele Identifier: PA2830057874
Gene: CEP192 HGNC NCBI

Linked Data

ClinVar Variation Id: 3142748
ClinVar RCV Id: RCV004436133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115518.3:p.Pro2170Ser
CA8900775
NM_032142.4:c.6508C>T