Canonical Allele Identifier: PA645411011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His25065Arg
CA1990089
NM_001267550.2:c.75194A>G