Canonical Allele Identifier: PA2825221761
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404397
ClinVar RCV Id: RCV000462264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Lys288Thr
CA16609965
NM_001001430.3:c.863A>C