Canonical Allele Identifier: PA916006025
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404397
ClinVar RCV Id: RCV000462264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Lys298Thr
CA16609965
NM_001276345.2:c.893A>C