Canonical Allele Identifier: PA2825224325
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202921
ClinVar RCV Id: RCV002651393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Phe82Tyr
CA344206644
NM_001001432.3:c.245T>A