Canonical Allele Identifier: PA2825225042
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Glu158Gly
CA089030
NM_001001432.3:c.473A>G