Canonical Allele Identifier: PA2826554765
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396943
ClinVar RCV Id: RCV001920084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Val94Ala
CA090143
NM_001276346.2:c.281T>C