Canonical Allele Identifier: PA211072
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 158262
ClinVar RCV Id: RCV000145634 RCV000270516 RCV000381261 RCV000969294 RCV004532649
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Gln1302Glu
CA211071
NM_014985.4:c.3904C>G