Canonical Allele Identifier: PA2826555204
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Asp86Ala
CA004228
NM_001276347.2:c.257A>C