Canonical Allele Identifier: PA2830226250
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile25613Thr
CA185350
NM_133432.3:c.76838T>C