Canonical Allele Identifier: PA2830218745
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47277
ClinVar RCV Id: RCV000040547 RCV000251867 RCV000714083 RCV001086284 RCV001133870 RCV001133871 RCV001133872 RCV001133873 RCV001133874 RCV001798176 RCV004534922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly14334Asp
CA140538
NM_133432.3:c.43001G>A