Canonical Allele Identifier: PA2830199561
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu23200Ile
CA1989796
NM_133378.4:c.69598C>A