Canonical Allele Identifier: PA2825224373
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2942386
ClinVar RCV Id: RCV003805600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Arg87Gly
CA344206581
NM_001001432.3:c.259C>G