Canonical Allele Identifier: PA2825224389
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304414
ClinVar RCV Id: RCV001752181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Lys88Glu
CA088114
NM_001001432.3:c.262A>G