Canonical Allele Identifier: PA645411097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val25903Ile
CA1989723
NM_001267550.2:c.77707G>A