Canonical Allele Identifier: PA178726
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_001254479.2:p.Gly18292Arg
CA178724
NM_001267550.2:c.54874G>C
CA349546891
NM_001267550.2:c.54874G>A