Canonical Allele Identifier: PA2741949361
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 2791255
ClinVar RCV Id: RCV003672364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.His986Pro
CA392343042
NM_014985.4:c.2957A>C