Canonical Allele Identifier: PA645484056
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316431
ClinVar RCV Id: RCV000310423 RCV000398792 RCV000481090 RCV000766784 RCV004021636 RCV004537787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Ser215Asn
CA7549074
NM_014985.4:c.644G>A