Canonical Allele Identifier: PA2826195732
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 1337199
ClinVar RCV Id: RCV001820213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181927.1:p.Met917Ile
CA7548479
NM_001194998.2:c.2751G>A
CA392343509
NM_001194998.2:c.2751G>C
CA392343510
NM_001194998.2:c.2751G>T