Canonical Allele Identifier: PA2830223389
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr21896Pro
CA1987436
NM_133432.3:c.65686A>C