Canonical Allele Identifier: PA2830200197
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 519031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile24702Thr
CA1989152
NM_133378.4:c.74105T>C