Canonical Allele Identifier: PA302731
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val10603Ile
CA302729
NM_001267550.2:c.31807G>A