Canonical Allele Identifier: PA2830227130
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 939688
ClinVar RCV Id: RCV001209123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26410Ile
CA349407142
NM_133432.3:c.79229C>T