Canonical Allele Identifier: PA2826411778
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val3342Ile
CA179186
NM_001256850.1:c.10024G>A