Canonical Allele Identifier: PA2829439279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47372
ClinVar RCV Id: RCV000040642 RCV000172633 RCV000296264 RCV000317619 RCV000348884 RCV000397192 RCV000467348 RCV000620048 RCV000388436 RCV000852500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg17344His
CA140828
NM_003319.4:c.52031G>A