Canonical Allele Identifier: PA297411
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Ala172Ser
CA004712
NM_001001430.3:c.514G>T