Canonical Allele Identifier: PA348786
Gene: E2F1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219310
ClinVar RCV Id: RCV000204567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005216.1:p.Arg166His
CA348785
NM_005225.3:c.497G>A