Canonical Allele Identifier: PA2829439793
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile18115Thr
CA140882
NM_003319.4:c.54344T>C