Canonical Allele Identifier: PA2829434552
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_003310.4:p.Gly9227Arg
CA178724
NM_003319.4:c.27679G>C
CA349546891
NM_003319.4:c.27679G>A