Canonical Allele Identifier: PA2826554513
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087171
ClinVar RCV Id: RCV002999960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Ala118Thr
CA344206396
NM_001276345.2:c.352G>A