Canonical Allele Identifier: PA2825153752
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735408
ClinVar RCV Id: RCV002364054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Glu138Gly
CA344205994
NM_000364.3:c.413A>G