Canonical Allele Identifier: PA2826421322
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr21942Lys
CA140591
NM_001256850.1:c.65825C>A