Canonical Allele Identifier: PA658670428
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452747
ClinVar RCV Id: RCV000646067 RCV001524972 RCV001836834 RCV003449496 RCV002323893 RCV003449495 RCV003449497
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Ile116Thr
CA344206413
NM_000364.3:c.347T>C
CA658656984
NM_000364.3:c.347_348delinsCT