Canonical Allele Identifier: PA2580177007
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2021831
ClinVar RCV Id: RCV002847316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34805Gly
CA349411785
NM_001267550.2:c.104413C>G