Canonical Allele Identifier: PA2826411768
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val3319Ile
CA346745
NM_001256850.1:c.9955G>A