Canonical Allele Identifier: PA140226
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile17902Thr
CA140224
NM_133378.4:c.53705T>C