Canonical Allele Identifier: PA645409325
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val8777Ile
CA2000027
NM_001267550.2:c.26329G>A