Canonical Allele Identifier: PA2830221077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile18240Thr
CA140882
NM_133432.3:c.54719T>C