Canonical Allele Identifier: PA2499279594
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004716
ClinVar RCV Id: RCV001301468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055771.4:p.Arg34Trp
CA6294327
NM_014956.5:c.100C>T