Canonical Allele Identifier: PA645411111
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val26022Ile
CA1989667
NM_001267550.2:c.78064G>A