Canonical Allele Identifier: PA139348
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46846
ClinVar RCV Id: RCV000040116 RCV000725691 RCV000456367 RCV002433509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val911Ile
CA139343
NM_133379.5:c.2731G>A