Canonical Allele Identifier: PA310513
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202861
ClinVar RCV Id: RCV000217890 RCV000727705 RCV001088038 RCV002336488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile25121Val
CA310511
NM_001267550.2:c.75361A>G