Canonical Allele Identifier: PA2825225051
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181622
ClinVar RCV Id: RCV000159303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Arg161Gly
CA004675
NM_001001432.3:c.481A>G