Canonical Allele Identifier: PA141106
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_001254479.2:p.Val29270Ile
CA141102
NM_001267550.2:c.87808G>A