Canonical Allele Identifier: PA645411112
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile26023Thr
CA1989666
NM_001267550.2:c.78068T>C