Canonical Allele Identifier: PA2830222745
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg20869Gln
CA141163
NM_133432.3:c.62606G>A