Canonical Allele Identifier: PA2826555077
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404397
ClinVar RCV Id: RCV000462264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Lys255Thr
CA16609965
NM_001276346.2:c.764A>C