Canonical Allele Identifier: PA2825220592
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_001001430.1:p.Arg139Ser
CA089867
NM_001001430.3:c.415C>A