Canonical Allele Identifier: PA2829363710
Gene: E2F4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3086745
ClinVar RCV Id: RCV004382123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001941.2:p.Ala239Gly
CA8103776
NM_001950.4:c.716C>G