Canonical Allele Identifier: PA2825222614
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2942251
ClinVar RCV Id: RCV003805465 RCV004006055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001431.1:p.Leu123Phe
CA344206202
NM_001001431.3:c.367C>T