Canonical Allele Identifier: PA1139698016
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 969453
ClinVar RCV Id: RCV001244808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Val131Leu
CA344206226
NM_001276345.2:c.391G>C