Canonical Allele Identifier: PA113359
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43636
ClinVar RCV Id: RCV000036583 RCV000159290 RCV000243733 RCV000468121 RCV001187129 RCV002470730 RCV003450693 RCV003450694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg140Cys
CA004443
NM_001276345.2:c.418C>T