Canonical Allele Identifier: PA261451
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Asp96Ala
CA004228
NM_000364.3:c.287A>C