Canonical Allele Identifier: PA2830224488
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47580
ClinVar RCV Id: RCV000040849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile23431Val
CA141413
NM_133432.3:c.70291A>G