Canonical Allele Identifier: PA100338
Gene: TBX22 HGNC NCBI

Linked Data

ClinVar Variation Id: 11334
ClinVar RCV Id: RCV000012087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001103348.1:p.Leu214Pro
CA121427
NM_001109878.2:c.641T>C