Canonical Allele Identifier: PA2826555233
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Ala104Glu
CA344206434
NM_001276347.2:c.311C>A