Canonical Allele Identifier: PA2826336715
Gene: CEP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 539588
ClinVar RCV Id: RCV000649345 RCV002530531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230705.1:p.Ser23Phe
CA6239364
NM_001243776.2:c.68C>T