Canonical Allele Identifier: PA2580252656
Gene: E2F4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2331421
ClinVar RCV Id: RCV004176938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001941.2:p.Pro342Thr
CA282313375
NM_001950.4:c.1024C>A