Canonical Allele Identifier: PA2825224321
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Asp81Ala
CA004228
NM_001001432.3:c.242A>C