Canonical Allele Identifier: PA2830235876
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser15662Tyr
CA185568
NM_133437.4:c.46985C>A