Canonical Allele Identifier: PA178822
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166007
ClinVar RCV Id: RCV000152342 RCV000532690 RCV000836249 RCV001130784 RCV001130783 RCV001133746 RCV001133747 RCV001133745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16827Gln
CA178820
NM_001267550.2:c.50480G>A