Canonical Allele Identifier: PA2829440043
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Tyr18497His
CA1989029
NM_003319.4:c.55489T>C