Canonical Allele Identifier: PA2826554860
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181622
ClinVar RCV Id: RCV000159303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Arg136Gly
CA004675
NM_001276346.2:c.406A>G