Canonical Allele Identifier: PA346747
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val3319Ile
CA346745
NM_001267550.2:c.9955G>A