Canonical Allele Identifier: PA2826489414
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 507466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1752His
CA2005205
NM_001267550.2:c.5255G>A