Canonical Allele Identifier: PA140666
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg21693Gln
CA140664
NM_133378.4:c.65078G>A