Canonical Allele Identifier: PA2826554506
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Ala114Glu
CA344206434
NM_001276345.2:c.341C>A