Canonical Allele Identifier: PA658659267
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35855Ile
CA60949238
NM_001267550.2:c.107564G>T