Canonical Allele Identifier: PA310928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202996
ClinVar RCV Id: RCV000184997 RCV002485254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val31296Ile
CA310926
NM_001267550.2:c.93886G>A