Canonical Allele Identifier: PA2825220326
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 684831
ClinVar RCV Id: RCV000845448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Glu119Gln
CA344206251
NM_001001430.3:c.355G>C