Canonical Allele Identifier: PA658813913
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 515003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13520Ile
CA349664595
NM_001267550.2:c.40558G>A