Canonical Allele Identifier: PA2829431669
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile3919Leu
CA2002660
NM_003319.4:c.11755A>C