Canonical Allele Identifier: PA2830220823
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly17869Ser
CA140856
NM_133432.3:c.53605G>A