Canonical Allele Identifier: PA140131
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg17137Cys
CA140129
NM_133378.4:c.51409C>T