Canonical Allele Identifier: PA310512
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_001243779.1:p.Ile23480Val
CA310511
NM_001256850.1:c.70438A>G