Canonical Allele Identifier: PA645409597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val12318Ile
CA1997327
NM_001267550.2:c.36952G>A