Canonical Allele Identifier: PA279264
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217496
ClinVar RCV Id: RCV000201435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Ile218Thr
CA279262
NM_000364.3:c.653T>C