Canonical Allele Identifier: PA2826554480
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2942386
ClinVar RCV Id: RCV003805600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg102Gly
CA344206581
NM_001276345.2:c.304C>G