Canonical Allele Identifier: PA2829363705
Gene: E2F4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3086743
ClinVar RCV Id: RCV004382121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001941.2:p.Gly5Val
CA396333697
NM_001950.4:c.14G>T