Canonical Allele Identifier: PA2825153833
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499363
ClinVar RCV Id: RCV003221664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg166Ser
CA344204658
NM_000364.3:c.498G>C
CA344204659
NM_000364.3:c.498G>T