Canonical Allele Identifier: PA2826555279
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 919022
ClinVar RCV Id: RCV001176946 RCV002223271 RCV003449581 RCV003449583 RCV003449582 RCV003769892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Arg130His
CA344205960
NM_001276347.2:c.389G>A