Canonical Allele Identifier: PA2825153665
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2943802
ClinVar RCV Id: RCV003803360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Asp108Val
CA344206500
NM_000364.3:c.323A>T