Canonical Allele Identifier: PA2826555235
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452747
ClinVar RCV Id: RCV000646067 RCV001524972 RCV001836834 RCV003449496 RCV002323893 RCV003449495 RCV003449497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Ile106Thr
CA344206413
NM_001276347.2:c.317T>C
CA658656984
NM_001276347.2:c.317_318delinsCT