Canonical Allele Identifier: PA2826195733
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 2229610
ClinVar RCV Id: RCV002712601 RCV003108168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Lys930Asn
CA7548474
NM_001194998.2:c.2790G>C
CA392343418
NM_001194998.2:c.2790G>T