Canonical Allele Identifier: PA261450
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Asp86Ala
CA004228
NM_001001430.3:c.257A>C