Canonical Allele Identifier: PA2830220203
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu16828Ile
CA1989796
NM_133432.3:c.50482C>A