Canonical Allele Identifier: PA2830212508
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val3273Ile
CA346745
NM_133432.3:c.9817G>A