Canonical Allele Identifier: PA2825153614
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717790
ClinVar RCV Id: RCV002304785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Asp99His
CA344206620
NM_000364.3:c.295G>C