Canonical Allele Identifier: PA2826541919
Gene: CEP164 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258862.1:p.Glu43Gln
CA382722023
NM_001271933.2:c.127G>C