Canonical Allele Identifier: PA2830212497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr3249Met
CA179196
NM_133432.3:c.9746C>T