Canonical Allele Identifier: PA645484087
Gene: CEP152 HGNC NCBI

Linked Data

ClinVar Variation Id: 316427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055800.2:p.Asn321Ser
CA7548987
NM_014985.4:c.962A>G