Canonical Allele Identifier: PA2826417686
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg15378Cys
CA1994260
NM_001256850.1:c.46132C>T