Canonical Allele Identifier: PA2573191536
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Glu173Gly
CA089030
NM_001276345.2:c.518A>G