Canonical Allele Identifier: PA2825224443
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2943802
ClinVar RCV Id: RCV003803360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Asp93Val
CA344206500
NM_001001432.3:c.278A>T