Canonical Allele Identifier: PA2580177011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2085391
ClinVar RCV Id: RCV002996247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34808Lys
CA349411768
NM_001267550.2:c.104422G>A