Canonical Allele Identifier: PA645408769
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264496
ClinVar RCV Id: RCV000252473 RCV000546848 RCV000615733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile3987Val
CA2002783
NM_001267550.2:c.11959A>G