Canonical Allele Identifier: PA2826554531
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075379
ClinVar RCV Id: RCV004016897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg140Leu
CA344205956
NM_001276345.2:c.419G>T