Canonical Allele Identifier: PA658815342
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518646
ClinVar RCV Id: RCV000619118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val22488Ile
CA349423707
NM_001267550.2:c.67462G>A