Canonical Allele Identifier: PA181674
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178179
ClinVar RCV Id: RCV000154906 RCV000477626 RCV000768882 RCV000733310 RCV002354369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile28668Thr
CA181672
NM_001267550.2:c.86003T>C