Canonical Allele Identifier: PA2830191308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys2196Tyr
CA10581902
NM_133378.4:c.6587G>A