Canonical Allele Identifier: PA2499244451
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171755
ClinVar RCV Id: RCV001525119 RCV002359149 RCV002471112 RCV003451791 RCV003451790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg136Ser
CA344206161
NM_001276345.2:c.408G>T
CA344206163
NM_001276345.2:c.408G>C