Canonical Allele Identifier: PA2830215495
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile8780Thr
CA310046
NM_133432.3:c.26339T>C