Canonical Allele Identifier: PA2830212129
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile2923Val
CA2004477
NM_133432.3:c.8767A>G