Canonical Allele Identifier: PA2826411638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys3109Arg
CA2004356
NM_001256850.1:c.9326A>G