Canonical Allele Identifier: PA645411750
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys28992Arg
CA1988400
NM_001267550.2:c.86974T>C