Canonical Allele Identifier: PA2826555565
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1329429
ClinVar RCV Id: RCV001799472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Lys280Asn
CA344201873
NM_001276347.2:c.840G>T
CA344201875
NM_001276347.2:c.840G>C