Canonical Allele Identifier: PA2826554529
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181616
ClinVar RCV Id: RCV000159289 RCV003765001 RCV003998389 RCV003453221 RCV003453222 RCV003453223 RCV004528900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Glu138Lys
CA004435
NM_001276345.2:c.412G>A