Canonical Allele Identifier: PA140025
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47106
ClinVar RCV Id: RCV000040376 RCV000172659 RCV000245388 RCV000270469 RCV000290334 RCV000324440 RCV000360425 RCV000384696 RCV001080060 RCV001170600 RCV004534910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys16877Arg
CA140022
NM_001256850.1:c.50630A>G