Canonical Allele Identifier: PA2825221798
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001431.1:p.Ile4Leu
CA026513
NM_001001431.3:c.10A>C
CA344209078
NM_001001431.3:c.10A>T