Canonical Allele Identifier: PA2826554847
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43648
ClinVar RCV Id: RCV000211867 RCV000459834 RCV000620577 RCV000624557 RCV002286700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Glu133del
CA004651
NM_001276346.2:c.397_399del
CA077423
NM_001276346.2:c.394G>T
CA344204544
NM_001276346.2:c.397G>T
CA344204579
NM_001276346.2:c.391G>T
CA344204597
NM_001276346.2:c.388G>T