Canonical Allele Identifier: PA113296
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177633
ClinVar RCV Id: RCV000476946 RCV000853450 RCV000845306 RCV001197200 RCV002255095 RCV001171166 RCV001699043 RCV002321633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Ala114Val
CA004337
NM_001276345.2:c.341C>T