Canonical Allele Identifier: PA2825153726
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1504448
ClinVar RCV Id: RCV002028797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Ser132Cys
CA344206209
NM_000364.3:c.395C>G