Canonical Allele Identifier: PA183098
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys35886Arg
CA183096
NM_001267550.2:c.107657A>G