Canonical Allele Identifier: PA658812451
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile3689Thr
CA2003996
NM_001267550.2:c.11066T>C