Canonical Allele Identifier: PA645408978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg5743Gln
CA2001876
NM_001267550.2:c.17228G>A