Canonical Allele Identifier: PA140298
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile18629Val
CA140295
NM_133378.4:c.55885A>G