Canonical Allele Identifier: PA916050677
Gene: CEP126 HGNC NCBI

Linked Data

ClinVar Variation Id: 774477
ClinVar RCV Id: RCV000954461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065853.3:p.Gln146Glu
CA6245211
NM_020802.3:c.436C>G