Canonical Allele Identifier: PA2830223074
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg21383Thr
CA310852
NM_133432.3:c.64148G>C