Canonical Allele Identifier: PA645409137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val7159Ile
CA2001018
NM_001267550.2:c.21475G>A