Canonical Allele Identifier: PA269843
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 132943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg154Trp
CA004554
NM_000364.3:c.460C>T