Canonical Allele Identifier: PA2826426307
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30436Gln
CA1986795
NM_001256850.1:c.91307G>A