Canonical Allele Identifier: PA2829433921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535392
ClinVar RCV Id: RCV000643347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val8087Ile
CA349585621
NM_003319.4:c.24259G>A