Canonical Allele Identifier: PA2826808507
Gene: TNNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302658
ClinVar RCV Id: RCV001756332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278703.1:p.His56Tyr
CA407435740
NM_001291774.2:c.166C>T