Canonical Allele Identifier: PA2825224381
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181637
ClinVar RCV Id: RCV000159330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.His86_Arg87insLeu
CA004260
NM_001001432.3:c.259_260insTTC