Canonical Allele Identifier: PA2828820133
Gene: BRD4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366220.1:p.Thr1309Ser
CA9264482
NM_001379291.1:c.3925A>T
CA404496453
NM_001379291.1:c.3926C>G