Canonical Allele Identifier: PA658815833
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu25768Ile
CA1989796
NM_001267550.2:c.77302C>A