Canonical Allele Identifier: PA2830216618
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg10765Cys
CA140129
NM_133432.3:c.32293C>T