Canonical Allele Identifier: PA2825222297
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 469519
ClinVar RCV Id: RCV000546244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001431.1:p.Asp86Asn
CA027243
NM_001001431.3:c.256G>A