Canonical Allele Identifier: PA658806249
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Lys1129Arg
CA2005562
NM_133379.5:c.3386A>G