Canonical Allele Identifier: PA2826520731
Gene: TBXT HGNC NCBI

Linked Data

ClinVar Variation Id: 126564
ClinVar RCV Id: RCV000114433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257413.1:p.His171Arg
CA151208
NM_001270484.2:c.512A>G