Canonical Allele Identifier: PA2825224431
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43631
ClinVar Variation Id: 2100789
ClinVar RCV Id: RCV003014581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Lys92Asn
CA004322
NM_001001432.3:c.276G>T
CA344206509
NM_001001432.3:c.276G>C