Canonical Allele Identifier: PA645380513
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404397
ClinVar RCV Id: RCV000462264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Lys295Thr
CA16609965
NM_000364.3:c.884A>C