Canonical Allele Identifier: PA2826730033
Gene: CENPE HGNC NCBI

Linked Data

ClinVar Variation Id: 434695
ClinVar RCV Id: RCV000500899 RCV000952897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273663.1:p.Arg1572Ser
CA3029758
NM_001286734.2:c.4716A>C
CA357778993
NM_001286734.2:c.4716A>T