Canonical Allele Identifier: PA141548
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47630
ClinVar RCV Id: RCV000040899 RCV000468674 RCV001133510 RCV001135007 RCV001133509 RCV001133511 RCV001133512 RCV001703915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu3097Pro
CA141544
NM_001267550.2:c.9290T>C