Canonical Allele Identifier: PA132841
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43631
ClinVar RCV Id: RCV000223847 RCV000788201 RCV000791922 RCV003450691 RCV003450690 RCV003450692 RCV003886369
ClinVar Variation Id: 2100789
ClinVar RCV Id: RCV003014581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Lys97Asn
CA004322
NM_001001430.3:c.291G>T
CA344206509
NM_001001430.3:c.291G>C