Canonical Allele Identifier: PA2826410902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 507466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg1752His
CA2005205
NM_001256850.1:c.5255G>A