Canonical Allele Identifier: PA658815779
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg25357Cys
CA1989958
NM_001267550.2:c.76069C>T