Canonical Allele Identifier: PA916019610
Gene: TBX22 HGNC NCBI

Linked Data

ClinVar Variation Id: 523404
ClinVar RCV Id: RCV000626748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290404.1:p.Lys30Gln
CA413740154
NM_001303475.1:c.88A>C