Canonical Allele Identifier: PA2825222642
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001431.1:p.Arg130Cys
CA004443
NM_001001431.3:c.388C>T