Canonical Allele Identifier: PA1139725913
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 885097
ClinVar RCV Id: RCV001116507 RCV001116506 RCV002558153 RCV002556464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Arg980Gln
CA269537959
NM_014985.4:c.2939G>A