Canonical Allele Identifier: PA915989776
Gene: TBX20 HGNC NCBI

Linked Data

ClinVar Variation Id: 4632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159692.1:p.Ile152Met
CA116972
NM_001166220.1:c.456C>G