Canonical Allele Identifier: PA2826554777
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075379
ClinVar RCV Id: RCV004016897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Arg100Leu
CA344205956
NM_001276346.2:c.299G>T