Canonical Allele Identifier: PA235076
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg25052His
CA235074
NM_001267550.2:c.75155G>A