Canonical Allele Identifier: PA2825224309
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Arg79Ser
CA004222
NM_001001432.3:c.237A>T
CA344206659
NM_001001432.3:c.237A>C