Canonical Allele Identifier: PA2825225080
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Ala167Ser
CA004712
NM_001001432.3:c.499G>T