Canonical Allele Identifier: PA211040
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 158246
ClinVar RCV Id: RCV000145617 RCV000344690 RCV000709779 RCV000906174 RCV004532646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Glu926Val
CA211038
NM_014985.4:c.2777A>T