Canonical Allele Identifier: PA2826337552
Gene: CEP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 191025
ClinVar RCV Id: RCV000171200 RCV001331874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230706.1:p.Arg30Pro
CA235845
NM_001243777.2:c.89G>C