Canonical Allele Identifier: PA185352
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile34553Thr
CA185350
NM_001267550.2:c.103658T>C