Canonical Allele Identifier: PA2829439729
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser18018Pro
CA181698
NM_003319.4:c.54052T>C