Canonical Allele Identifier: PA2499279591
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060292
ClinVar RCV Id: RCV001369702 RCV004037091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055771.4:p.Pro5Thr
CA6294295
NM_014956.5:c.13C>A