Canonical Allele Identifier: PA096789
Gene: TBX20 HGNC NCBI

Linked Data

ClinVar Variation Id: 4632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071121.1:p.Ile152Met
CA116972
NM_001077653.2:c.456C>G