Canonical Allele Identifier: PA916051286
Gene: TBX22 HGNC NCBI

Linked Data

ClinVar Variation Id: 368671
ClinVar RCV Id: RCV000330393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058650.1:p.Ala515Glu
CA10461423
NM_016954.2:c.1544C>A