Canonical Allele Identifier: PA2830214506
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp7060His
CA309902
NM_133432.3:c.21178G>C