Canonical Allele Identifier: PA139322
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46839
ClinVar RCV Id: RCV000040109 RCV000471292 RCV000620387 RCV000725605 RCV000770154 RCV001135012 RCV001135014 RCV001135013 RCV001135010 RCV001135011 RCV004534885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val896Ile
CA139318
NM_001267550.2:c.2686G>A