Canonical Allele Identifier: PA141467
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47596
ClinVar RCV Id: RCV000040865 RCV000172610 RCV000341836 RCV000298721 RCV000338814 RCV000387355 RCV000401107 RCV000620090 RCV000768849 RCV001081784 RCV004534949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg30180Cys
CA141465
NM_133378.4:c.90538C>T