Canonical Allele Identifier: PA2825224847
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115456
ClinVar RCV Id: RCV003046468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Arg134Gly
CA344205821
NM_001001432.3:c.400C>G