Canonical Allele Identifier: PA2826493600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr2545Ile
CA61006134
NM_001267550.2:c.7634C>T