Canonical Allele Identifier: PA658667164
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val26369Ile
CA1989522
NM_001267550.2:c.79105G>A