Canonical Allele Identifier: PA2830237462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 519031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile18397Thr
CA1989152
NM_133437.4:c.55190T>C