Canonical Allele Identifier: PA2825224263
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Pro75Thr
CA004164
NM_001001432.3:c.223C>A