Canonical Allele Identifier: PA2825220200
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087171
ClinVar RCV Id: RCV002999960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Ala108Thr
CA344206396
NM_001001430.3:c.322G>A