Canonical Allele Identifier: PA2826416352
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg12798Cys
CA1995898
NM_001256850.1:c.38392C>T