Canonical Allele Identifier: PA113393
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12411
ClinVar RCV Id: RCV000013222 RCV000036622 RCV000159322 RCV000162331 RCV000148898 RCV000157540 RCV000203739 RCV000248304 RCV000755702 RCV000771167 RCV000768493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg288Cys
CA005245
NM_001276345.2:c.862C>T