Canonical Allele Identifier: PA2573068875
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.His91Tyr
CA344206593
NM_001276347.2:c.271C>T