Canonical Allele Identifier: PA2825153622
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.His101Tyr
CA344206593
NM_000364.3:c.301C>T