Canonical Allele Identifier: PA2829792172
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 434735
ClinVar RCV Id: RCV000501448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Leu1512Ile
CA392333845
NM_014985.4:c.4534C>A