Canonical Allele Identifier: PA2825222211
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001431.1:p.Pro80Thr
CA004164
NM_001001431.3:c.238C>A