Canonical Allele Identifier: PA658809277
Gene: CEP57 HGNC NCBI

Linked Data

ClinVar Variation Id: 539588
ClinVar RCV Id: RCV000649345 RCV002530531
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055494.2:p.Ser32Phe
CA6239364
NM_014679.5:c.95C>T