Canonical Allele Identifier: PA2829792109
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Ile1336Thr
CA7548145
NM_014985.4:c.4007T>C