Canonical Allele Identifier: PA2826104611
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_001165556.1:p.Gln74_Gln75dup
CA4108305
NM_001172085.2:c.216_221dup
CA4108338
NM_001172085.2:c.218_219insACAGCA
CA572352912
NM_001172085.2:c.221_222insGCAACA
CA2578803238
NM_001172085.2:c.220_225dup