Canonical Allele Identifier: PA658665785
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17019Cys
CA1994260
NM_001267550.2:c.51055C>T