Canonical Allele Identifier: PA2825556465
Gene: TBX22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685164
ClinVar RCV Id: RCV002248891 RCV002488629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001103348.1:p.Arg151Leu
CA10461235
NM_001109878.2:c.452G>T