Canonical Allele Identifier: PA2573068877
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310834
ClinVar RCV Id: RCV001761004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Lys97del
CA2573051461
NM_001276347.2:c.289_291del