Canonical Allele Identifier: PA310057
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202711
ClinVar RCV Id: RCV000184623 RCV002485244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18065Cys
CA310055
NM_001267550.2:c.54193C>T