Canonical Allele Identifier: PA2830226942
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg26224His
CA311232
NM_133432.3:c.78671G>A