Canonical Allele Identifier: PA2826520772
Gene: TBXT HGNC NCBI

Linked Data

ClinVar Variation Id: 218621
ClinVar RCV Id: RCV000203203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257413.1:p.Ser338Leu
CA249409
NM_001270484.2:c.1013C>T