Canonical Allele Identifier: PA141104
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47469
ClinVar RCV Id: RCV000040738 RCV000118785 RCV000307938 RCV000403035 RCV000397868 RCV000313315 RCV000370289 RCV001170318 RCV002354214 RCV001080518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val26702Ile
CA141102
NM_133378.4:c.80104G>A