Canonical Allele Identifier: PA139907
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47066
ClinVar RCV Id: RCV000040336 RCV000118765 RCV000852845 RCV001129509 RCV001136507 RCV001084228 RCV001129508 RCV001129510 RCV001129511 RCV002426577 RCV004534905 RCV001798159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17618Cys
CA139904
NM_001267550.2:c.52852C>T