Canonical Allele Identifier: PA645410425
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20003His
CA1992564
NM_001267550.2:c.60008G>A