Canonical Allele Identifier: PA645411279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg27176Leu
CA1989195
NM_001267550.2:c.81527G>T