Canonical Allele Identifier: PA261457
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43629
ClinVar RCV Id: RCV000036576 RCV000159284 RCV000468546 RCV000619398 RCV001258056 RCV003450686 RCV003450687 RCV003450688
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Arg94Leu
CA004302
NM_001001430.3:c.281G>T