Canonical Allele Identifier: PA183460
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr22921Ile
CA183458
NM_001267550.2:c.68762C>T