Canonical Allele Identifier: PA916005691
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 469519
ClinVar RCV Id: RCV000546244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Asp96Asn
CA027243
NM_001276345.2:c.286G>A