Canonical Allele Identifier: PA285783
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr24866Ala
CA285779
NM_001267550.2:c.74596A>G