Canonical Allele Identifier: PA211046
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 95651
ClinVar RCV Id: RCV000145619 RCV000515271 RCV000723661 RCV001116508 RCV004542793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Trp960Arg
CA211044
NM_014985.4:c.2878T>C
CA392343234
NM_014985.4:c.2878T>A