Canonical Allele Identifier: PA658665031
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val7976Ile
CA2000545
NM_001267550.2:c.23926G>A