Canonical Allele Identifier: PA2826555365
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181622
ClinVar RCV Id: RCV000159303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Arg166Gly
CA004675
NM_001276347.2:c.496A>G