Canonical Allele Identifier: PA2830210143
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile741Thr
CA2005850
NM_133432.3:c.2222T>C