Canonical Allele Identifier: PA2826554469
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202921
ClinVar RCV Id: RCV002651393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Phe97Tyr
CA344206644
NM_001276345.2:c.290T>A