Canonical Allele Identifier: PA113467
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235065
ClinVar RCV Id: RCV000223859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Phe120Val
CA10581127
NM_001276345.2:c.358T>G