Canonical Allele Identifier: PA2826418608
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys17083Arg
CA1993298
NM_001256850.1:c.51248A>G