Canonical Allele Identifier: PA141053
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr26256Ile
CA141051
NM_133378.4:c.78767C>T