Canonical Allele Identifier: PA2580183885
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735408
ClinVar RCV Id: RCV002364054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Glu98Gly
CA344205994
NM_001276346.2:c.293A>G