Canonical Allele Identifier: PA2826336713
Gene: CEP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 191025
ClinVar RCV Id: RCV000171200 RCV001331874
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230705.1:p.Arg21Pro
CA235845
NM_001243776.2:c.62G>C