Canonical Allele Identifier: PA2826555352
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43648
ClinVar RCV Id: RCV000211867 RCV000459834 RCV000620577 RCV000624557 RCV002286700
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Glu163del
CA004651
NM_001276347.2:c.487_489del
CA077423
NM_001276347.2:c.484G>T
CA344204544
NM_001276347.2:c.487G>T
CA344204579
NM_001276347.2:c.481G>T
CA344204597
NM_001276347.2:c.478G>T