Canonical Allele Identifier: PA139651
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46964
ClinVar RCV Id: RCV000040234 RCV000230470 RCV001588857 RCV002399386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile11772Thr
CA139649
NM_133378.4:c.35315T>C