Canonical Allele Identifier: PA2741997745
Gene: BRD4 HGNC NCBI
ClinVar RCV:
RCV003707581
ClinVar Variation:
2878318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_490597.1:p.Thr1309Ser
CA9264482
NM_058243.3:c.3925A>T
CA404496453
NM_058243.3:c.3926C>G