Canonical Allele Identifier: PA2826555209
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43625
ClinVar RCV Id: RCV000036570
ClinVar Variation Id: 666939
ClinVar RCV Id: RCV000825476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Asp88Glu
CA004247
NM_001276347.2:c.264T>G
CA344206634
NM_001276347.2:c.264T>A