Canonical Allele Identifier: PA2825153606
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2023506
ClinVar RCV Id: RCV002858000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Phe97_Asp98delinsSerLeuHisProArgTrpArgGluSer
CA2580061936
NM_000364.3:c.290_293delinsCTCTCCATCCCCGATGGAGAGAGAG