Canonical Allele Identifier: PA645380037
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430390
ClinVar RCV Id: RCV000493712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg149Ser
CA089867
NM_000364.3:c.445C>A