Canonical Allele Identifier: PA2826411368
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr2545Ile
CA61006134
NM_001256850.1:c.7634C>T