Canonical Allele Identifier: PA184457
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val13226Ile
CA184456
NM_133378.4:c.39676G>A