Canonical Allele Identifier: PA658653990
Gene: CENPE HGNC NCBI

Linked Data

ClinVar Variation Id: 445884
ClinVar RCV Id: RCV000514886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001804.2:p.Ile1402Val
CA3029880
NM_001813.3:c.4204A>G