Canonical Allele Identifier: PA2826541909
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258862.1:p.Gln27Lys
CA229370653
NM_001271933.2:c.79C>A