Canonical Allele Identifier: PA913196837
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629593
ClinVar RCV Id: RCV000774302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Lys125Ile
CA344206298
NM_000364.3:c.374A>T