Canonical Allele Identifier: PA283029
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46806
ClinVar RCV Id: RCV000040076 RCV000231488 RCV000291931 RCV000344859 RCV000390703 RCV000346806 RCV000404062 RCV001081637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr9040Ile
CA283026
NM_001256850.1:c.27119C>T