Canonical Allele Identifier: PA261471
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_000355.2:p.Glu173del
CA004651
NM_000364.3:c.517_519del
CA077423
NM_000364.3:c.514G>T
CA344204544
NM_000364.3:c.517G>T
CA344204579
NM_000364.3:c.511G>T
CA344204597
NM_000364.3:c.508G>T