Canonical Allele Identifier: PA2826884046
Gene: TBX22 HGNC NCBI

Linked Data

ClinVar Variation Id: 11329
ClinVar RCV Id: RCV000012082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290404.1:p.Thr140Met
CA121423
NM_001303475.1:c.419C>T