Canonical Allele Identifier: PA282732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46648
ClinVar RCV Id: RCV000039918 RCV000226134 RCV000290608 RCV000304112 RCV000345615 RCV000349032 RCV000402296 RCV000769068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val6286Ile
CA282728
NM_001267550.2:c.18856G>A