Canonical Allele Identifier: PA139652
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_001254479.2:p.Ile14340Thr
CA139649
NM_001267550.2:c.43019T>C