Canonical Allele Identifier: PA284528
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47821
ClinVar RCV Id: RCV000041090 RCV000463695 RCV000619735 RCV000770115 RCV001839792 RCV001839793 RCV001839794 RCV001839795 RCV002227056 RCV004541204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr3761Ile
CA284526
NM_001256850.1:c.11282C>T