Canonical Allele Identifier: PA915970142
Gene: CENPE HGNC NCBI

Linked Data

ClinVar Variation Id: 787273
ClinVar RCV Id: RCV000969477 RCV001819094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001804.2:p.Lys638Glu
CA3030398
NM_001813.3:c.1912A>G