Canonical Allele Identifier: PA2826541948
Gene: CEP164 HGNC NCBI

Linked Data

ClinVar Variation Id: 37296
ClinVar RCV Id: RCV000030835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258862.1:p.Arg93Trp
CA130150
NM_001271933.2:c.277C>T