Canonical Allele Identifier: PA645411126
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26134His
CA1989607
NM_001267550.2:c.78401G>A