Canonical Allele Identifier: PA645409921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr15801Ile
CA1995050
NM_001267550.2:c.47402C>T