Canonical Allele Identifier: PA2825225917
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452905
ClinVar RCV Id: RCV000522658 RCV004003647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Trp281Leu
CA344201828
NM_001001432.3:c.842G>T