Canonical Allele Identifier: PA915988722
Gene: CEP43 HGNC NCBI

Linked Data

ClinVar Variation Id: 786767
ClinVar RCV Id: RCV000968880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008976.1:p.Ala277Pro
CA4095547
NM_007045.4:c.829G>C