Canonical Allele Identifier: PA311120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203060
ClinVar RCV Id: RCV000185076 RCV003137748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys33528Glu
CA311118
NM_001267550.2:c.100582A>G