Canonical Allele Identifier: PA2830197979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg19428Cys
CA1991600
NM_133378.4:c.58282C>T