Canonical Allele Identifier: PA1139698209
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 836384
ClinVar RCV Id: RCV001037499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Lys97Glu
CA344206524
NM_001276347.2:c.289A>G