Canonical Allele Identifier: PA140667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47317
ClinVar RCV Id: RCV000040587 RCV000172641 RCV000288602 RCV000343679 RCV000349884 RCV000388861 RCV000397203 RCV001080138 RCV002336145 RCV003149657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22620Gln
CA140664
NM_001256850.1:c.67859G>A