Canonical Allele Identifier: PA178725
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165972
ClinVar Variation Id: 2438169
ClinVar RCV Id: RCV003137334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly15724Arg
CA178724
NM_133378.4:c.47170G>C
CA349546891
NM_133378.4:c.47170G>A