Canonical Allele Identifier: PA645484084
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316429
ClinVar RCV Id: RCV000265493 RCV000320543 RCV000420504 RCV000965295 RCV002522801 RCV004537785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Lys309Gln
CA7548993
NM_014985.4:c.925A>C