Canonical Allele Identifier: PA2825153613
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2437140
ClinVar RCV Id: RCV003141060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Asp99Asn
CA090282
NM_000364.3:c.295G>A