Canonical Allele Identifier: PA2826554767
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Asp95Ala
CA004228
NM_001276346.2:c.284A>C