Canonical Allele Identifier: PA2826554527
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735342
ClinVar RCV Id: RCV002364027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Glu138Gln
CA344206001
NM_001276345.2:c.412G>C