Canonical Allele Identifier: PA2830227592
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 968568
ClinVar RCV Id: RCV001243734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser26893Lys
CA1139657376
NM_133432.3:c.80678_80679delinsAA