Canonical Allele Identifier: PA658665301
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val10722Ile
CA1998714
NM_001267550.2:c.32164G>A