Canonical Allele Identifier: PA2826554774
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Arg100Cys
CA004443
NM_001276346.2:c.298C>T