Canonical Allele Identifier: PA139751
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47007
ClinVar RCV Id: RCV000040277 RCV000206445 RCV000283374 RCV000253777 RCV000291644 RCV000343176 RCV000346585 RCV000382285 RCV000769010 RCV001081905 RCV004541157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15731Cys
CA139747
NM_001267550.2:c.47191C>T