Canonical Allele Identifier: PA2825153599
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2939571
ClinVar RCV Id: RCV003794737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg94Ile
CA344206660
NM_000364.3:c.281G>T