Canonical Allele Identifier: PA645409305
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg8646His
CA2000097
NM_001267550.2:c.25937G>A