Canonical Allele Identifier: PA645380009
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 389145
ClinVar RCV Id: RCV000441620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg141Gly
CA16603524
NM_000364.3:c.421C>G