Canonical Allele Identifier: PA2830227132
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser26412Pro
CA60953469
NM_133432.3:c.79234T>C