Canonical Allele Identifier: PA2826421299
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val21908Ile
CA1990755
NM_001256850.1:c.65722G>A