Canonical Allele Identifier: PA2829445705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val26138Ala
CA1985231
NM_003319.4:c.78413T>C