Canonical Allele Identifier: PA2826729953
Gene: CENPE HGNC NCBI

Linked Data

ClinVar Variation Id: 787273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273663.1:p.Lys613Glu
CA3030398
NM_001286734.2:c.1837A>G