Canonical Allele Identifier: PA2826730016
Gene: CENPE HGNC NCBI
ClinVar RCV:
RCV000514886
ClinVar Variation:
445884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273663.1:p.Ile1377Val
CA3029880
NM_001286734.2:c.4129A>G