Canonical Allele Identifier: PA658667131
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile26144Thr
CA1989604
NM_001267550.2:c.78431T>C