Canonical Allele Identifier: PA2828820094
Gene: BRD4 HGNC NCBI
ClinVar RCV:
RCV002756246
ClinVar Variation:
1979935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366220.1:p.Ala1189Val
CA9264605
NM_001379291.1:c.3566C>T