Canonical Allele Identifier: PA916066996
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Cys9745Arg
CA1993375
NM_133437.4:c.29233T>C