Canonical Allele Identifier: PA2829441138
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg20278His
CA141113
NM_003319.4:c.60833G>A