Canonical Allele Identifier: PA184458
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val15794Ile
CA184456
NM_001267550.2:c.47380G>A