Canonical Allele Identifier: PA2829443913
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Cys24344Tyr
CA302391
NM_003319.4:c.73031G>A