Canonical Allele Identifier: PA2826555350
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43647
ClinVar RCV Id: RCV000036595 RCV000225721 RCV004018798 RCV000703215 RCV001798104 RCV002470731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Arg159Gln
CA004638
NM_001276347.2:c.476G>A