Canonical Allele Identifier: PA658654490
Gene: TBP HGNC NCBI

Linked Data

ClinVar Variation Id: 445790
ClinVar RCV Id: RCV000514133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003185.1:p.Gln94_Gln95dup
CA4108305
NM_003194.5:c.276_281dup
CA4108338
NM_003194.5:c.278_279insACAGCA
CA572352912
NM_003194.5:c.281_282insGCAACA
CA2578803238
NM_003194.5:c.280_285dup