Canonical Allele Identifier: PA2830190665
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile787Thr
CA2005850
NM_133378.4:c.2360T>C