Canonical Allele Identifier: PA179379
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166331
ClinVar RCV Id: RCV000152517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val1024Ile
CA179376
NM_133378.4:c.3070G>A